This list of
rare diseases was originally taken from the
NIH public domain resource at
http://ord.aspensys.com/diseases.asp .
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
- C syndrome[?]
- C1 esterase deficiency, (type 2 with ascites)[?]
- Cacchi Ricci disease[?]
- CACH syndrome[?]
- Cacophobia[?]
- Cafe au lait spots syndrome[?]
- Caffey disease[?]
- CAHMR syndrome[?]
- Calcinosis-Raynaud phenomenon-sclerodactyly-telangiectasia[?]
- Calciphylaxis[?]
- Calculi[?]
- Calderon Gonzalez Cantu syndrome[?]
- Calloso genital dysplasia[?]
- Callus disease[?]
- Calpainopathy[?]
- Calvarial hyperostosis[?]
- Camera Marugo -Cohen syndrome[?]
- Camfak syndrome[?]
- Campomelia Cumming type[?]
- Camptobrachydactyly[?]
- Camptocormism[?]
- Camptodactyly fibrous tissue hyperplasia skeletal dysplasia[?]
- Camptodactyly joint contractures facial skeletal dysplasia[?]
- Camptodactyly overgrowth unusual facies[?]
- Camptodactyly syndrome Guadalajara type 1[?]
- Camptodactyly syndrome Guadalajara type 2[?]
- Camptodactyly taurinuria[?]
- Camptodactyly vertebral fusion[?]
- Camptomelic syndrome[?]
- Camurati Engelmann disease[?]
- Canavan leukodystrophy[?]
- Candidiasis familial chronic[?]
- Canga's bead symptom
- Cantalamessa Baldini Ambrosi syndrome[?]
- Cantu Sanchez Corona Fragoso syndrome[?]
- Cantu Sanchez Corona Garcia syndrome[?]
- Cantu Sanchez Corona Hernandes syndrome[?]
- Capillary leak syndrome with monoclonal gammopathy[?]
- Capillary venous leptomeningeal angiomatosis[?]
- Capos syndrome[?]
- Caratolo Cilio Pessagno syndrome[?]
- Carbamoyl phosphate synthetase deficiency[?]
- Carbamoyl-phosphate synthase I deficiency disease (ornithine carbamoyl phosphate deficiency)[?]
- Carbohydrate deficient glycoprotein syndrome[?]
- Carbon baby syndrome[?]
- Carbonic anhydrase II deficiency[?]
- Carcinoid syndrome[?]
- Carcinoma of the vocal tract[?]
- Carcinoma, squamous cell of head and neck[?]
- Carcinoma, squamous cell[?]
- Carcinophobia[?]
- Cardiac and laterality defects[?]
- Cardiac conduction defect, familial[?]
- Cardiac diverticulum[?]
- Cardiac hydatid cysts with intracavitary expansion[?]
- Cardiac malformation[?]
- Cardiac valvular dysplasia, X-linked[?]
- Cardioauditory syndrome of Sanchez- Cascos[?]
- Cardioauditory syndrome[?]
- Cardiofacial syndrome short limbs[?]
- Cardio-facio-cutaneous syndrome[?]
- Cardiogenital syndrome[?]
- Cardiomelic syndrome Stratton Koehler type[?]
- Cardiomyopathic lentiginosis[?]
- Cardiomyopathy cataract hip spine disease[?]
- Cardiomyopathy diabetes deafness[?]
- Cardiomyopathy dilated with conduction defect type 1[?]
- Cardiomyopathy dilated with conduction defect type 2[?]
- Cardiomyopathy due to anthracyclines[?]
- Cardiomyopathy hearing loss type t RNA lysine gene mutation[?]
- Cardiomyopathy hypogonadism metabolic anomalies[?]
- Cardiomyopathy spherocytosis[?]
- Cardiomyopathy, familial dilated[?]
- Cardiomyopathy, familial hypertrophic[?]
- Cardiomyopathy, fatal fetal, due to myocardial calcification[?]
- Cardiomyopathy, Hypertrophic, Familial[?]
- Cardiomyopathy, X linked, fatal infantile[?]
- Cardiophobia[?]
- Cardioskeletal myopathy-neutropenia[?]
- Cardiospasm[?]
- Carey Fineman Ziter syndrome[?]
- Carnevale Canun Mendoza syndrome[?]
- Carnevale Hernandez Castillo syndrome[?]
- Carnevale Krajewska Fischetto syndrome[?]
- Carney syndrome[?]
- Carnitine palmitoyl transferase 1 deficiency[?]
- Carnitine palmitoyl transferase 2 deficiency[?]
- Carnitine palmitoyl transferase deficiency[?]
- Carnitine transporter deficiency[?]
- Carnitine-acylcarnitine translocase deficiency[?]
- Carnophobia[?]
- Carnosinase deficiency[?]
- Carnosinemia[?]
- Caroli disease[?]
- Carpal deformity migrognathia microstomia[?]
- Carpal tunnel syndrome
- Carpenter Hunter type[?]
- Carpenter syndrome[?]
- Carpo tarsal osteolysis recessive[?]
- Carpotarsal osteochondromatosis[?]
- Carrington syndrome[?]
- Cartilage hair hypoplasia like syndrome[?]
- Cartilaginous neoplasms[?]
- Cartwright Nelson Fryns syndrome[?]
- Cassia Stocco Dos Santos syndrome[?]
- Castleman's disease[?]
- Castro Gago Pombo Novo syndrome[?]
- Cat cry syndrome[?]
- Cat Eye syndrome[?]
- Cat Rodrigues syndrome[?]
- Cat Scratch Disease[?]
- Catagelophobia[?]
- Catapedaphobia[?]
- Cataract ,congenital ichthyosis[?]
- Cataract aberrant oral frenula growth retardation[?]
- Cataract anterior polar dominant[?]
- Cataract ataxia deafness[?]
- Cataract cardiomyopathy[?]
- Cataract congenital autosomal dominant[?]
- Cataract congenital dominant non nuclear[?]
- Cataract congenital Volkmann type[?]
- Cataract congenital with microphthalmia[?]
- Cataract dental syndrome[?]
- Cataract Hutterite type[?]
- Cataract hypertrichosis mental retardation[?]
- Cataract mental retardation hypogonadism[?]
- Cataract microcornea syndrome[?]
- Cataract microphthalmia septal defect[?]
- Cataract skeletal anomalies[?]
- Cataract, alopecia, sclerodactyly[?]
- Cataract, congenital, with microcornea or slight microphthalmia[?]
- Cataract, total congenital[?]
- Cataract-glaucoma[?]
- CATCH 22 syndrome
- Catecholamine hypertension[?]
- Catel Manzke syndrome[?]
- Caudal appendage deafness[?]
- Caudal duplication[?]
- Caudal regression syndrome[?]
- Causalgia[?]
- Cavernous hemangioma[?]
- Cavernous lymphangioma[?]
- Cayler syndrome[?]
- CCA syndrome[?]
- Ccge syndrome[?]
- CCHS[?]
- CDG syndrome type 1A
- CDG syndrome type 1B[?]
- CDG syndrome type 1C[?]
- CDG syndrome type 2[?]
- CDG syndrome type 3[?]
- CDG syndrome type 4[?]
- CDG syndrome
- CDK4 linked melanoma[?]
- Cecato De lima Pinheiro syndrome[?]
- Celiac disease epilepsy occipital calcifications[?]
- Celiac sprue[?]
- Cenani Lenz syndactylism
- Cennamo Gangemi syndrome[?]
- Central core disease[?]
- Central diabetes insipidus[?]
- Central nervous system protozoal infections[?]
- Central serous chorioretinopathy[?]
- Central type neurofibromatosis[?]
- Centromeric instability immunodeficiency syndrome[?]
- Centronuclear myopathy, congenital[?]
- Centrotemporal epilepsy[?]
- Cephalopolysyndactyly[?]
- Ceramidase deficiency[?]
- Ceramide trihexosidosis[?]
- Ceraunophobia[?]
- Cerebellar agenesis[?]
- Cerebellar ataxia areflexia pes cavus optic atrophy[?]
- Cerebellar ataxia ectodermal dysplasia[?]
- Cerebellar ataxia infantile with progressive external ophthalmoplegia[?]
- Cerebellar ataxia, dominant pure[?]
- Cerebellar ataxia[?]
- Cerebellar degeneration, subacute[?]
- Cerebellar degeneration[?]
- Cerebellar hypoplasia endosteal sclerosis[?]
- Cerebellar hypoplasia tapetoretinal degeneration[?]
- Cerebellar hypoplasia[?]
- Cerebellar parenchymal degeneration[?]
- Cerebelloolivary atrophy[?]
- Cerebelloparenchymal disorder 3[?]
- Cerebellum agenesis hydrocephaly[?]
- Cerebral Amyloid Angiopathy, Familial[?]
- Cerebral amyloid angiopathy[?]
- Cerebral aneurysm
- Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy[?]
- Cerebral calcification cerebellar hypoplasia[?]
- Cerebral calcifications opalescent teeth phosphaturia[?]
- Cerebral cavernous malformation[?]
- Cerebral cavernous malformations[?]
- Cerebral gigantism jaw cysts[?]
- Cerebral gigantism[?]
- Cerebral malformations hypertrichosis claw hands[?]
- Cerebral palsy
- Cerebral ventricle neoplasm[?]
- Cerebro facio articular syndrome[?]
- Cerebro facio thoracic dysplasia[?]
- Cerebro oculo dento auriculo skeletal syndrome[?]
- Cerebro oculo genital syndrome[?]
- Cerebro oculo skeleto renal syndrome[?]
- Cerebro reno digital syndrome[?]
- Cerebroarthrodigital syndrome[?]
- Cerebro-costo-mandibular syndrome[?]
- Cerebro-oculo-facio-skeletal syndrome[?]
- Cerebroretinal vasculopathy[?]
- Ceroid lipofuscinose, neuronal 1, infantile[?]
- Ceroid lipofuscinose, neuronal 2, late infantile[?]
- Ceroid lipofuscinose, neuronal 3, juvenile[?]
- Ceroid lipofuscinose, neuronal 4, adult type[?]
- Ceroid lipofuscinose, neuronal 5, late infantile,[?]
- Ceroid lipofuscinose, neuronal 6, late infantile[?]
- Ceroid lipofuscinose, neuronal[?]
- Ceroid lipofuscinosis, neuronal 4[?]
- Cervical cancer
- Cervical hypertrichosis neuropathy[?]
- Cervical hypertrichosis peripheral neuropathy[?]
- Cervical ribs sprengel anomaly polydactyly[?]
- Cervical vertebral fusion[?]
- Cervicooculoacoustic syndrome[?]
- Chagas disease
- Chalazion[?]
- Chanarin disease[?]
- Chanarin Dorfman syndrome ichthyosis[?]
- Chandler's syndrome[?]
- Chands syndrome[?]
- Chang Davidson Carlson syndrome[?]
- Chaotic atrial tachycardia[?]
- Char syndrome[?]
- Charcot disease[?]
- Charcot Marie tooth disease deafness dominant type[?]
- Charcot Marie tooth disease deafness mental retardation[?]
- Charcot Marie Tooth disease deafness recessive type[?]
- Charcot Marie Tooth type 1 aplasia cutis congenita[?]
- Charcot-Marie-Tooth disease, X-linked type 2, recessive[?]
- Charcot-Marie-Tooth disease, X-linked type 3, recessive[?]
- Charcot-Marie-Tooth disease type 1A[?]
- Charcot-Marie-Tooth disease type 1B[?]
- Charcot-Marie-Tooth disease type 1C[?]
- Charcot-Marie-Tooth disease type 2A[?]
- Charcot-Marie-Tooth disease type 2B1[?]
- Charcot-Marie-Tooth disease type 2B2[?]
- Charcot-Marie-Tooth disease type 2C[?]
- Charcot-Marie-Tooth disease type 2D[?]
- Charcot-Marie-Tooth disease type 4A[?]
- Charcot-Marie-Tooth disease type 4B[?]
- Charcot-Marie-Tooth disease with ptosis and parkinsonism[?]
- Charcot-Marie-Tooth disease, intermediate form[?]
- Charcot-Marie-Tooth disease, neuronal, type A[?]
- Charcot-Marie-Tooth disease, neuronal, type B[?]
- Charcot-Marie-Tooth disease, neuronal, type D[?]
- Charcot-Marie-tooth disease[?]
- Charcot-Marie-Tooth peroneal muscular atrophy, X-linked[?]
- CHARGE Association[?]
- Charlie M syndrome[?]
- Chavany-Brunhes syndrome[?]
- Chediak-Higashi syndrome[?]
- Cheilitis glandularis[?]
- Chemke Oliver Mallek syndrome[?]
- Chemodectoma[?]
- Chemophobia
- Chen Kung Ho Kaufman Mcalister syndrome[?]
- Cherubism[?]
- Chiari type 1 malformation[?]
- Chiari-Frommel syndrome[?]
- Chikungunya[?]
- CHILD syndrome ichthyosis[?]
- Childhood disintegrative disorder[?]
- Childhood pustular psoriasis[?]
- Chionophobia[?]
- Chiraptophobia[?]
- Chirophobia[?]
- Chitayat Haj Chahine syndrome[?]
- Chitayat Meunier Hodgkinson syndrome[?]
- Chitayat Moore Del Bigio syndrome[?]
- Chitty Hall Baraitser syndrome[?]
- Chitty Hall Webb syndrome[?]
- Chlamydia
- Chlamydial and Gonococcal Conjunctivitis[?]
- Choanal atresia deafness cardiac defects dysmorphia[?]
- Cholangiocarcinoma[?]
- Cholangitis, primary sclerosing[?]
- Cholecystitis[?]
- Choledochal cyst, hand malformation[?]
- Cholemia, familial[?]
- Cholera
- Cholerophobia[?]
- Cholestasis pigmentary retinopathy cleft palate[?]
- Cholestasis, progressive familial intrahepatic 1[?]
- Cholestasis, progressive familial intrahepatic 2[?]
- Cholestasis, progressive familial intrahepatic 3[?]
- Cholestasis, progressive familial intrahepatic[?]
- Cholestasis[?]
- Cholestatic jaundice renal tubular insufficiency[?]
- Cholesterol ester storage disease[?]
- Cholesterol esterification disorder[?]
- Cholesterol pneumonia[?]
- Chondroblastoma (benign)[?]
- Chondrocalcinosis familial articular[?]
- Chondrocalcinosis[?]
- Chondrodysplasia lethal recessive[?]
- Chondrodysplasia pseudohermaphrodism syndrome[?]
- Chondrodysplasia punctata 1, x-linked recessive[?]
- Chondrodysplasia punctata with steroid sulfatase deficiency[?]
- Chondrodysplasia punctata, brachytelephalangic[?]
- Chondrodysplasia punctata, Sheffield type[?]
- Chondrodysplasia punctata[?]
- Chondrodysplasia situs inversus imperforate anus polydactyly[?]
- Chondrodysplasia, Grebe type[?]
- Chondrodystrophy[?]
- Chondroectodermal dysplasia[?]
- Chondroma (benign)[?]
- Chondromalacia[?]
- Chondromatosis (benign)[?]
- Chondrosarcoma (malignant)[?]
- Chondrysplasia punctata, humero-metacarpal type[?]
- Chordoma[?]
- Chorea acanthocytosis[?]
- Chorea familial benign[?]
- Chorea minor[?]
- Chorea
- Choreoacanthocytosis amyotrophic[?]
- Choreoathetosis familial paroxysmal[?]
- Choriocarcinoma[?]
- Chorioretinitis
- Chorioretinopathy dominant form microcephaly[?]
- Choroid plexus cyst[?]
- Choroid Plexus neoplasms[?]
- Choroidal atrophy alopecia[?]
- Choroideremia hypopituitarism[?]
- Choroideremia[?]
- Choroiditis, serpiginous[?]
- Choroiditis[?]
- Choroido cerebral calcification syndrome infantile[?]
- Chorophobia[?]
- Christian Demyer Franken syndrome[?]
- Christian Johnson Angenieta syndrome[?]
- Christian syndrome[?]
- Christianson Fourie syndrome[?]
- Christmas disease
- Chromomycosis[?]
- Chromophobe renal carcinoma[?]
- Chromophobia[?]
- Chromosomal triplication[?]
- Chromosome 1 ring[?]
- Chromosome 1, 1p36 deletion syndrome[?]
- Chromosome 1, deletion q21 q25[?]
- Chromosome 1, duplication 1p21 p32[?]
- Chromosome 1, monosomy 1p[?]
- Chromosome 1, monosomy 1p22 p13[?]
- Chromosome 1, monosomy 1p31 p22[?]
- Chromosome 1, monosomy 1p32[?]
- Chromosome 1, monosomy 1p34 p32[?]
- Chromosome 1, monosomy 1q25 q32[?]
- Chromosome 1, monosomy 1q32 q42[?]
- Chromosome 1, monosomy 1q4[?]
- Chromosome 1, q42 11 q42 12 duplication[?]
- Chromosome 1, trisomy 1q32 qter[?]
- Chromosome 1, trisomy 1q42 qter[?]
- Chromosome 1, uniparental disomy 1q12 q21[?]
- Chromosome 10 ring[?]
- Chromosome 10, distal trisomy 10q[?]
- Chromosome 10, monosomy 10p[?]
- Chromosome 10, monosomy 10q[?]
- Chromosome 10, trisomy 10p[?]
- Chromosome 10, trisomy 10pter p13[?]
- Chromosome 10, trisomy 10q[?]
- Chromosome 10, uniparental disomy of[?]
- Chromosome 10p terminal deletion syndrome[?]
- Chromosome 11, deletion 11p[?]
- Chromosome 11, partial trisomy 11q[?]
- Chromosome 11-14 translocation[?]
- Chromosome 11p, partial deletion[?]
- Chromosome 11q partial deletion[?]
- Chromosome 11q trisomy[?]
- Chromosome 12 ring[?]
- Chromosome 12, 12p trisomy[?]
- Chromosome 12, trisomy 12q[?]
- Chromosome 12p deletion[?]
- Chromosome 12p partial deletion[?]
- Chromosome 13 duplication[?]
- Chromosome 13 ring[?]
- Chromosome 13, partial monosomy 13q[?]
- Chromosome 13p duplication[?]
- Chromosome 13q deletion[?]
- Chromosome 13q trisomy[?]
- Chromosome 13q-mosaicism[?]
- Chromosome 14 ring[?]
- Chromosome 14 trisomy[?]
- Chromosome 14, deletion 14q, partial duplication 14p[?]
- Chromosome 14, trisomy mosaic[?]
- Chromosome 14q, partial deletions[?]
- Chromosome 14q, proximal duplication[?]
- Chromosome 14q, terminal deletion[?]
- Chromosome 14q, terminal duplication[?]
- Chromosome 15 ring[?]
- Chromosome 15, distal trisomy 15q[?]
- Chromosome 15, trisomy mosaicism[?]
- Chromosome 15q, partial deletion
- Chromosome 15q, tetrasomy[?]
- Chromosome 15q, trisomy
- Chromosome 16, trisomy 16p[?]
- Chromosome 16, trisomy 16q[?]
- Chromosome 16, trisomy[?]
- Chromosome 16, uniparental disomy[?]
- Chromosome 17 trisomy[?]
- Chromosome 17 deletion[?]
- Chromosome 17 ring[?]
- Chromosome 17, deletion 17q23 q24[?]
- Chromosome 17, trisomy 17p[?]
- Chromosome 17, trisomy 17p11 2[?]
- Chromosome 17, trisomy 17q22[?]
- Chromosome 18 long arm deletion syndrome[?]
- Chromosome 18 mosaic monosomy[?]
- Chromosome 18 ring[?]
- Chromosome 18, deletion 18q23[?]
- Chromosome 18, monosomy 18p[?]
- Chromosome 18, tetrasomy 18p[?]
- Chromosome 18, trisomy 18p[?]
- Chromosome 18, trisomy 18q[?]
- Chromosome 18, trisomy[?]
- Chromosome 19 ring[?]
- Chromosome 19, trisomy 19q[?]
- Chromosome 1q, duplication 1q12 q21[?]
- Chromosome 2, monosomy 2p22[?]
- Chromosome 2, monosomy 2pter p24[?]
- Chromosome 2, monosomy 2q[?]
- Chromosome 2, monosomy 2q24[?]
- Chromosome 2, monosomy 2q37[?]
- Chromosome 2, trisomy 2p[?]
- Chromosome 2, Trisomy 2p13 p21[?]
- Chromosome 2, trisomy 2pter p24[?]
- Chromosome 2, trisomy 2q[?]
- Chromosome 2, trisomy 2q37[?]
- Chromosome 20 ring[?]
- Chromosome 20, deletion 20p[?]
- Chromosome 20, duplication 20p[?]
- Chromosome 20, trisomy[?]
- Chromosome 21 monosomy[?]
- Chromosome 21 ring[?]
- Chromosome 21, monosomy 21q22[?]
- Chromosome 21, tetrasomy 21q[?]
- Chromosome 21, uniparental disomy of[?]
- Chromosome 22 ring[?]
- Chromosome 22 trisomy mosaic[?]
- Chromosome 22, microdeletion 22 q11
- Chromosome 22, monosome mosaic[?]
- Chromosome 22, trisomy q11 q13[?]
- Chromosome 22, trisomy[?]
- Chromosome 3 duplication syndrome[?]
- Chromosome 3, monosomy 3p[?]
- Chromosome 3, monosomy 3p14 p11[?]
- Chromosome 3, monosomy 3p2[?]
- Chromosome 3, monosomy 3p25[?]
- Chromosome 3, monosomy 3q13[?]
- Chromosome 3, monosomy 3q21 23[?]
- Chromosome 3, monosomy 3q27[?]
- Chromosome 3, trisomy 3p[?]
- Chromosome 3, trisomy 3p25[?]
- Chromosome 3, trisomy 3q[?]
- Chromosome 3, trisomy 3q13 2 q25[?]
- Chromosome 3, Trisomy 3q2[?]
- Chromosome 4 ring[?]
- Chromosome 4 short arm deletion[?]
- Chromosome 4, monosomy 4p14 p16[?]
- Chromosome 4, monosomy 4q[?]
- Chromosome 4, monosomy 4q32[?]
- Chromosome 4, monosomy distal 4q[?]
- Chromosome 4, partial trisomy distal 4q[?]
- Chromosome 4, Trisomy 4p[?]
- Chromosome 4, trisomy 4q[?]
- Chromosome 4, trisomy 4q21[?]
- Chromosome 4, trisomy 4q25 qter[?]
- Chromosome 5, monosomy 5q35[?]
- Chromosome 5, trisomy 5p[?]
- Chromosome 5, trisomy 5pter p13 3[?]
- Chromosome 5, trisomy 5q[?]
- Chromosome 5, uniparental disomy[?]
- Chromosome 6 ring[?]
- Chromosome 6, deletion 6q13 q15[?]
- Chromosome 6, monosomy 6p23[?]
- Chromosome 6, monosomy 6q[?]
- Chromosome 6, monosomy 6q1[?]
- Chromosome 6, monosomy 6q2[?]
- Chromosome 6, partial trisomy 6q[?]
- Chromosome 6, trisomy 6p[?]
- Chromosome 6, trisomy 6q[?]
- Chromosome 7 ring[?]
- Chromosome 7, monosomy 7q2[?]
- Chromosome 7, monosomy 7q21[?]
- Chromosome 7, monosomy 7q3[?]
- Chromosome 7, monosomy[?]
- Chromosome 7, partial monosomy 7p[?]
- Chromosome 7, trisomy 7p[?]
- Chromosome 7, trisomy 7p13 p12 2[?]
- Chromosome 7, trisomy 7q[?]
- Chromosome 7, trisomy mosaic[?]
- Chromosome 8 deletion[?]
- Chromosome 8 ring[?]
- Chromosome 8, monosomy 8p[?]
- Chromosome 8, monosomy 8p2[?]
- Chromosome 8, monosomy 8p23 1[?]
- Chromosome 8, monosomy 8q[?]
- Chromosome 8, mosaic trisomy[?]
- Chromosome 8, partial trisomy[?]
- Chromosome 8, trisomy 8p[?]
- Chromosome 8, trisomy 8q[?]
- Chromosome 8, trisomy[?]
- Chromosome 9 inversion or duplication[?]
- Chromosome 9 Ring[?]
- Chromosome 9, duplication 9q21[?]
- Chromosome 9, monosomy 9p[?]
- Chromosome 9, partial monosomy 9p[?]
- Chromosome 9, partial trisomy 9p[?]
- Chromosome 9, tetrasomy 9p[?]
- Chromosome 9, trisomy 9q[?]
- Chromosome 9, trisomy 9q32[?]
- Chromosome 9, trisomy mosaic[?]
- Chromosome 9, trisomy[?]
- Chromosomes 1 and 2, monosomy 2q duplication 1p[?]
- Chronic berylliosis[?]
- Chronic demyelinizing neuropathy with IgM monoclonal[?]
- Chronic erosive gastritis[?]
- Chronic fatigue immune dysfunction syndrome[?]
- Chronic granulomatous disease[?]
- Chronic hiccup[?]
- Chronic inflammatory demyelinating polyneuropathy[?]
- Chronic lymphocytic leukemia[?]
- Chronic myelogenous leukemia[?]
- Chronic myelomonocytic leukemia[?]
- Chronic necrotizing vasculitis[?]
- Chronic neutropenia[?]
- Chronic polyradiculoneuritis[?]
- Chronic recurrent multifocal osteomyelitis[?]
- Chronic renal failure[?]
- Chronic spasmodic dysphonia[?]
- Chronic, infantile, neurological, cutaneous, articular syndrome[?]
- Chronomentrophobia[?]
- Chudley Lowry Hoar syndrome[?]
- Chudley Rozdilsky syndrome[?]
- Chudley-Mccullough syndrome[?]
- Churg-Strauss syndrome[?]
- Chylous ascites[?]
- Cicatricial pemphigoid[?]
- Ciguatera fish poisoning[?]
- Ciliary discoordination, due to random ciliary orientation[?]
- Ciliary dyskinesia, due to transposition of ciliary microtubules[?]
- Ciliary dyskinesia-bronchiectasis[?]
- Cilliers Beighton syndrome[?]
- Circumscribed cutaneous aplasia of the vertex[?]
- Circumscribed disseminated keratosis Jadassohn Lew type[?]
- Citrullinemia[?]
- Clarkson disease[?]
- Clayton Smith Donnai syndrome[?]
- Cleft hand absent tibia[?]
- Cleft lip and palate malrotation cardiopathy[?]
- Cleft lip and/or palate with mucous cysts of lower[?]
- Cleft lip palate abnormal thumbs microcephaly[?]
- Cleft lip palate deafness sacral lipoma[?]
- Cleft lip palate dysmorphism Kumar type[?]
- Cleft lip palate ectrodactyly[?]
- Cleft lip palate incisor and finger anomalies[?]
- Cleft lip palate mental retardation corneal opacity[?]
- Cleft lip palate oligodontia syndactyly pili torti[?]
- Cleft lip palate pituitary deficiency[?]
- Cleft lip palate-tetraphocomelia[?]
- Cleft lip with or without cleft palate[?]
- Cleft lip
- Cleft lower lip cleft lateral canthi chorioretinal[?]
- Cleft palate cardiac defect ectrodactyly[?]
- Cleft palate colobomata radial synostosis deafness[?]
- Cleft palate heart disease polydactyly absent tibia[?]
- Cleft palate lateral synechia syndrome[?]
- Cleft palate short stature vertebral anomalies[?]
- Cleft palate stapes fixation oligodontia[?]
- Cleft palate X linked[?]
- Cleft palate
- Cleft tongue syndrome[?]
- Cleft upper lip median cutaneous polyps[?]
- Clefting ectropion conical teeth[?]
- Cleidocranial dysplasia micrognathia absent thumbs[?]
- Cleidocranial dysplasia[?]
- Cleisiophobia[?]
- Climacophobia[?]
- Clinophobia
- Cloacal exstrophy[?]
- Clouston syndrome[?]
- Cloverleaf skull bone dysplasia[?]
- Cloverleaf skull micromelia thoracic dysplasia[?]
- Cluster headache[?]
- CMV antenatal infection[?]
- Coach syndrome[?]
- Coal worker's pneumoconiosis[?]
- Coarctation of aorta dominant[?]
- Coarse face hypotonia constipation[?]
- Coats disease[?]
- Cocaine antenatal infection[?]
- Cocaine fetopathy[?]
- Cochin Jewish Disorder[?]
- Cockayne syndrome type 1[?]
- Cockayne syndrome type 2[?]
- Cockayne syndrome type 3[?]
- Cockayne's syndrome[?]
- Codas syndrome[?]
- Coenzyme Q cytochrome c reductase deficiency of[?]
- Coffin-Lowry syndrome[?]
- Coffin-Siris syndrome[?]
- COFS syndrome[?]
- Cogan-Reese syndrome[?]
- Cogan's syndrome[?]
- Cohen Hayden syndrome[?]
- Cohen Lockood Wyborney syndrome[?]
- Cohen syndrome[?]
- Colavita Kozlowski syndrome[?]
- Cold agglutination syndrome[?]
- Cold agglutinin disease[?]
- Cold antibody hemolytic anemia[?]
- Cold contact urticaria[?]
- Cold urticaria[?]
- Cole carpenter syndrome[?]
- Coleman Randall syndrome[?]
- colitis[?]
- Collagen disorder[?]
- Collagenous colitis[?]
- Collins Pope syndrome[?]
- Collins Sakati syndrome[?]
- Coloboma chorioretinal cerebellar vermis aplasia[?]
- Coloboma hair abnormality[?]
- Coloboma of choroid and retina[?]
- Coloboma of eye lens[?]
- Coloboma of iris[?]
- Coloboma of lens ala nasi[?]
- Coloboma of macula type B brachydactyly[?]
- Coloboma of macula[?]
- Coloboma of optic nerve[?]
- Coloboma of optic papilla[?]
- Coloboma porencephaly hydronephrosis[?]
- Coloboma uveal with cleft lip palate and mental retardation[?]
- Coloboma, ocular[?]
- Colobomata unilobar lung heart defect[?]
- Colobomatous microphthalmia heart disease hearing [?]
- Colobomatous microphthalmia[?]
- Colon cancer, familial nonpolyposis[?]
- Colonic atresia[?]
- Colonic malakoplakia[?]
- Colorado tick fever[?]
- Colver Steer Godman syndrome[?]
- Combarros Calleja Leno syndrome[?]
- Combined hyperlipidemia, familial[?]
- Common mesentery[?]
- Common variable immunodeficiency[?]
- Compartment syndrome
- Complement component 2 deficiency[?]
- Complement component receptor 1[?]
- Complete atrioventricular canal[?]
- Complex 1 mitochondrial respiratory chain deficiency[?]
- Complex 2 mitochondrial respiratory chain deficiency[?]
- Complex 3 mitochondrial respiratory chain deficiency[?]
- Complex 4 mitochondrial respiratory chain deficiency[?]
- Complex 5 mitochondrial respiratory chain deficiency[?]
- Conductive deafness malformed external ear[?]
- Conductive hearing loss[?]
- Condyloma acuminatum[?]
- Condyloma[?]
- Cone dystrophy[?]
- Cone rod dystrophy amelogenesis imperfecta[?]
- Cone rod dystrophy[?]
- Congenital absence of the uterus and vagina[?]
- Congenital adrenal hyperplasia type 1[?]
- Congenital adrenal hyperplasia type 2[?]
- Congenital adrenal hyperplasia type 3[?]
- Congenital adrenal hyperplasia type 4[?]
- Congenital adrenal hyperplasia type 5[?]
- Congenital adrenal hyperplasia[?]
- Congenital afibrinogenemia[?]
- Congenital alopecia X linked[?]
- Congenital amputation[?]
- Congenital aneurysms of the great vessels[?]
- Congenital antithrombin III deficiency[?]
- Congenital aplastic anemia[?]
- Congenital arteriovenous shunt[?]
- Congenital articular rigidity[?]
- Congenital benign spinal muscular atrophy dominant[?]
- Congenital brain disorder[?]
- Congenital bronchobiliary fistula[?]
- Congenital cardiovascular disorder[?]
- Congenital cardiovascular malformations[?]
- Congenital cardiovascular shunt[?]
- Congenital constricting band[?]
- Congenital contractual arachnodactyly[?]
- Congenital contractures[?]
- Congenital craniosynostosis maternal hyperthyroiditis[?]
- Congenital cystic adenomatoid malformation[?]
- Congenital cystic eye multiple ocular and intracranial anomalies[?]
- Congenital cytomegalovirus[?]
- Congenital deafness[?]
- Congenital diaphragmatic hernia[?]
- Congenital erythropoietic porphyria[?]
- Congenital facial diplegia[?]
- Congenital fiber type disproportion[?]
- Congenital gastrointestinal disorder[?]
- Congenital generalized fibromatosis[?]
- Congenital giant megaureter[?]
- Congenital heart block[?]
- Congenital heart disease ptosis hypodontia craniostosis[?]
- Congenital heart disease radio ulnar synostosis mental retardation[?]
- Congenital heart disorder[?]
- Congenital heart septum defect[?]
- Congenital hemidysplasia with ichtyosiform erythroderma and limbs defects[?]
- Congenital hemolytic anemia[?]
- Congenital hepatic fibrosis[?]
- Congenital hepatic porphyria[?]
- Congenital herpes simplex[?]
- Congenital hypomyelination neuropathy[?]
- Congenital hypothyroidism[?]
- Congenital hypotrichosis milia[?]
- Congenital ichthyosis, microcephalus, quadriplegia[?]
- Congenital ichthyosis[?]
- Congenital ichtyosiform erythroderma[?]
- Congenital kidney disorder[?]
- Congenital lobar emphysema[?]
- Congenital megacolon[?]
- Congenital megalo-ureter[?]
- Congenital mesoblastic nephroma[?]
- Congenital microvillous atrophy[?]
- Congenital mitral malformation[?]
- Congenital mitral stenosis[?]
- Congenital mixovirus[?]
- Congenital mumps[?]
- Congenital muscular dystrophy syringomyelia[?]
- Congenital myopathy[?]
- Congenital nephrotic syndrome, Finnish type[?]
- Congenital nonhemolytic jaundice[?]
- Congenital rubella[?]
- Congenital short bowel[?]
- Congenital short femur[?]
- Congenital skeletal disorder[?]
- Congenital skin disorder[?]
- Congenital spherocytic anemia[?]
- Congenital spherocytic hemolytic anemia[?]
- Congenital stenosis of cervical medullary canal[?]
- Congenital sucrose isomaltose malabsorption[?]
- Congenital syphilis[?]
- Congenital toxoplasmosis[?]
- Congenital unilateral pulmonary hypoplasia[?]
- Congenital vagal hyperreflexivity[?]
- Congenital varicella syndrome[?]
- Conjunctivitis ligneous[?]
- Conjunctivitis with Pseudomembrane[?]
- Conjunctivitis
- Connective tissue dysplasia Spellacy type[?]
- Connexin 26 anomaly[?]
- Conn's syndrome[?]
- Conotruncal heart malformations[?]
- Conradi-Hünermann syndrome[?]
- Constitutional growth delay[?]
- Constrictive bronchiolitis[?]
- Continuous muscle fiber activity hereditary[?]
- Continuous spike-wave during slow sleep syndrome[?]
- Contractural arachnodactyly[?]
- Contractures ectodermal dysplasia cleft lip palate[?]
- Contractures hyperkeratosis lethal[?]
- Contractures of feet-muscle atrophy-oculomotor apraxia[?]
- Conversion disorder[?]
- Convulsions benign familial neonatal dominant form[?]
- Convulsions benign familial neonatal[?]
- Cooks syndrome[?]
- Cooley's anemia[?]
- Copper deficiency familial benign[?]
- Copper transport disease[?]
- Coprastasophobia[?]
- Coprophobia[?]
- Coproporhyria[?]
- Cor biloculare[?]
- Cor triatriatum[?]
- Cormier Rustin Munnich syndrome[?]
- Corneal anesthesia deafness mental retardation[?]
- Corneal cerebellar syndrome[?]
- Corneal crystals myopathy neuropathy[?]
- Corneal dystrophy epithelial short stature[?]
- Corneal dystrophy ichthyosis microcephaly mental retardation[?]
- Corneal dystrophy perceptive deafness[?]
- Corneal dystrophy pigmentary anomaly malabsorption[?]
- Corneal dystrophy[?]
- Corneal endothelium dystrophy[?]
- Cornelia de Lange syndrome[?]
- Corneodermatoosseous syndrome[?]
- Coronal synostosis syndactyly jejunal atresia[?]
- Coronaro-cardiac fistula[?]
- Coronary arteries congenital malformation[?]
- Coronary artery aneurysm[?]
- Corpus callosum agenesis double urinary collecting[?]
- Corpus callosum agenesis neuronopathy[?]
- Corpus callosum agenesis of blepharophimosis Robin type[?]
- Corpus callosum agenesis of with chorioretinal abnormalities[?]
- Corpus callosum agenesis polysyndactyly[?]
- Corpus callosum agenesis[?]
- Corpus callosum dysgenesis cleft spasm[?]
- Corpus callosum dysgenesis hypopituitarism[?]
- Corpus callosum dysgenesis X linked recessive[?]
- Corrected transposition[?]
- Corsello Opitz syndrome[?]
- Cortada Koussef Matsumoto syndrome[?]
- Cortes Lacassie syndrome[?]
- Cortical blindness mental retardation polydactyly[?]
- Cortical degeneration of the cerebellum parenchymatous[?]
- Cortical hyperostosis syndactyly[?]
- Corticobasal degeneration[?]
- Costello syndrome[?]
- Costocoracoid ligament congenitally short[?]
- Cote Adamopoulos Pantelakis syndrome[?]
- Cote Katsantoni syndrome[?]
- Cousin Walbraum Cegarra syndrome[?]
- Covesdem syndrome[?]
- Cowchock Wapner Kurtz syndrome[?]
- Cowden's disease[?]
- Cowpox
- Coxoauricular syndrome[?]
- Cramer Niederdellmann syndrome[?]
- Cramp-fasciculations syndrome[?]
- Crandall syndrome[?]
- Crane-Heise syndrome[?]
- Cranio osteoarthropathy[?]
- Cranioacrofacial syndrome[?]
- Craniodiaphyseal dysplasia[?]
- Craniodigital syndrome mental retardation[?]
- Cranioectodermal dysplasia[?]
- Craniofacial and osseous defects mental retardation[?]
- Craniofacial and skeletal defects[?]
- Craniofacial deafness hand syndrome[?]
- Craniofacial dysostosis arthrogryposis progeroid appearance[?]
- Craniofacial dysostosis[?]
- Craniofacial dysynostosis[?]
- Craniofaciocardioskeletal syndrome[?]
- Craniofaciocervical osteoglyphic dysplasia[?]
- Craniofrontonasal dysplasia[?]
- Craniofrontonasal syndrome Teebi type[?]
- Craniometaphyseal dysplasia dominant type[?]
- Craniometaphyseal dysplasia recessive type[?]
- Craniomicromelic syndrome[?]
- Craniostenosis cataract[?]
- Craniostenosis with congenital heart disease mental retardation[?]
- Craniostenosis[?]
- Craniosynostosis alopecia brain defect[?]
- Craniosynostosis arthrogryposis cleft palate[?]
- Craniosynostosis autosomal dominant[?]
- Craniosynostosis cleft lip palate arthrogryposis[?]
- Craniosynostosis contractures cleft[?]
- Craniosynostosis exostoses nevus epibulbar dermoid[?]
- Craniosynostosis fibular aplasia[?]
- Craniosynostosis Fontaine type[?]
- Craniosynostosis Maroteaux Fonfria type[?]
- Craniosynostosis mental retardation clefting syndrome[?]
- Craniosynostosis mental retardation heart defects[?]
- Craniosynostosis Philadelphia type[?]
- Craniosynostosis radial aplasia syndrome[?]
- Craniosynostosis synostoses hypertensive nephropathy[?]
- Craniosynostosis Warman type[?]
- Craniosynostosis, sagittal, with Dandy-Walker malformation and hydrocephalus[?]
- Craniosynostosis[?]
- Craniotelencephalic dysplasia[?]
- Crawfurd syndrome[?]
- Creatine deficiency[?]
- Creeping disease[?]
- CREST syndrome[?]
- Cretinism athyreotic[?]
- Cretinism
- Cri du chat syndrome
- Crigler Najjar syndrome type I[?]
- Crisponi syndrome[?]
- Criss cross syndrome[?]
- Criswick-Schepens syndrome[?]
- Crohn's disease of the esophagus[?]
- Crohn's disease
- Crome syndrome[?]
- Cronkhite-Canada disease[?]
- Crossed polydactyly type 1[?]
- Crossed polysyndactyly[?]
- Crow-Fukase syndrome[?]
- Cryoglobulinemia[?]
- Cryophobia[?]
- Cryptococcosis[?]
- Cryptogenic organized pneumopathy[?]
- Cryptomicrotia brachydactyly syndrome excess fingers[?]
- Cryptomicrotia brachydactyly syndrome[?]
- Cryptophthalmos-syndactyly syndrome[?]
- Cryptorchidism arachnodactyly mental retardation[?]
- Cryptosporidiosis[?]
- Cryroglobulinemia[?]
- Crystal deposit disease[?]
- Crystallophobia[?]
- Culler Jones syndrome[?]
- Curly hair ankyloblepharon nail dysplasia syndrome[?]
- Currarino triad[?]
- Curry Hall syndrome[?]
- Curth-Macklin type ichthyosis hystrix[?]
- Curtis Rogers Stevenson syndrome[?]
- Cushing syndrome, familial[?]
- Cushing's symphalangism[?]
- Cushing's syndrome
- Cutaneous anthrax[?]
- Cutaneous larva migrans[?]
- Cutaneous lupus erythematosus[?]
- Cutaneous photosensitivity colitis lethal[?]
- Cutaneous T-cell lymphoma[?]
- Cutaneous vascularitis[?]
- Cutis Gyrata syndrome of Beare and Stevenson[?]
- Cutis gyratum acanthosis nigricans craniosynostosis[?]
- Cutis laxa , recessive[?]
- Cutis laxa corneal clouding mental retardation[?]
- Cutis laxa osteoporosis[?]
- Cutis laxa with joint laxity and retarded development[?]
- Cutis laxa, dominant type[?]
- Cutis laxa, recessive type 1[?]
- Cutis laxa, recessive type 2[?]
- Cutis laxa[?]
- Cutis marmorata telangiectatica congenita[?]
- Cutis verticis gyrata mental deficiency[?]
- Cutis verticis gyrata thyroid aplasia mental retardation[?]
- Cutis verticis gyrata[?]
- Cutler Bass Romshe syndrome[?]
- Cyclic neutropenia[?]
- Cyclic vomiting syndrome[?]
- Cyclosporosis[?]
- Cypress facial neuromusculoskeletal syndrome[?]
- Cystathionine beta synthetase deficiency[?]
- Cystic adenomatoid malformation of lung[?]
- Cystic angiomatosis of bone, diffuse[?]
- Cystic fibrosis gastritis megaloblastic anemia[?]
- Cystic fibrosis
- Cystic hamartoma of lung and kidney[?]
- Cystic hygroma lethal cleft palate[?]
- Cystic hygroma[?]
- Cystic medial necrosis of aorta[?]
- Cystin transport, protein defect of[?]
- Cystinosis[?]
- Cystinuria[?]
- Cystinuria-lysinuria[?]
- Cytochrome C oxidase deficiency[?]
- Cytomegalic inclusion disease[?]
- Cytomegalovirus
- Cytoplasmic body myopathy[?]
- Czeizel Losonci syndrome[?]
- Czeizel syndrome[?]