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
- N acetyltransferase deficiency[?]
- N syndrome[?]
- N-acetyl glutamate synthetase deficiency[?]
- N-acetyl-alpha-D-galactosaminidase[?]
- N-acetyl-glucosamine-6-sulfate sulfatase deficiency[?]
- NADH CoQ reductase, deficiency of[?]
- NADH cytochrome B5 reductase deficiency[?]
- Naegeli syndrome[?]
- Naguib syndrome[?]
- Nail-patella syndrome[?]
- Nakajo Nishimura syndrome[?]
- Nakajo syndrome[?]
- Nakamura Osame syndrome[?]
- NAME syndrome[?]
- Nance-Horan syndrome[?]
- Nanism due to growth hormone combined deficiency[?]
- Nanism due to growth hormone isolated deficiency with X linked hypogammaglobulinemia[?]
- Nanism due to growth hormone resistance[?]
- Narcolepsy
- Narcolepsy-Cataplexy[?]
- Narrow oral fissure short stature cone shaped epiphyses[?]
- Nasodigitoacoustic syndrome[?]
- Nasopalpebral lipoma coloboma syndrome[?]
- Nasopharyngeal carcinoma[?]
- Nasopharyngeal teratoma Dandy Walker diaphragmatic hernia[?]
- Natal teeth intestinal pseudoobstruction patent ductus[?]
- Nathalie syndrome[?]
- Native american myopathy[?]
- Navajo poikiloderma[?]
- Necrophobia[?]
- Necrotizing encephalopathy, infantile subacute[?]
- Negative rheumatoid factor polyarthritis[?]
- Neisseria meningitidis[?]
- Nelson syndrome[?]
- Nemaline myopathy 1, Autosomal Dominant[?]
- Nemaline Myopathy 2, Autosomal Recessive[?]
- Nemaline Myopathy, Amish Type[?]
- Neonatal hemochromatosis[?]
- Neonatal hepatitis[?]
- Neonatal herpes[?]
- Neonatal ovarian cyst[?]
- Neonatal transient jaundice[?]
- Neopharmaphobia[?]
- Neophobia[?]
- Nephophobia[?]
- Nephroblastomatosis,fetal ascites,macrosomia and Wilm's tumor[?]
- Nephrocalcinosis[?]
- Nephrogenic diabetes insipidus[?]
- Nephrolithiasis type 2[?]
- Nephronophthisis familial adult spastic quadriparesis[?]
- Nephropathy deafness hyperparathyroidism[?]
- Nephropathy familial with hyperuricemia[?]
- Nephropathy, familial with gout[?]
- Nephrosclerosis[?]
- Nephrosis deafness urinary tract digital malformation[?]
- Nephrosis neuronal dysmigration syndrome[?]
- Nephrotic syndrome ocular anomalies[?]
- Nephrotic syndrome, idiopathic, steroid-resistant[?]
- Nerve sheath neoplasm[?]
- Nesidioblastosis of pancreas[?]
- Netherton syndrome ichthyosis[?]
- Neu Laxova syndrome[?]
- Neuhauser Daly Magnelli syndrome[?]
- Neuhauser Eichner Opitz syndrome[?]
- Neural crest tumor[?]
- Neural tube defect, folate-sensitive[?]
- Neural tube defects X linked[?]
- Neuraminidase beta-galactosidase deficiency[?]
- Neuraminidase deficiency[?]
- Neurasthenia[?]
- Neurilemmomatosis[?]
- Neuritis with brachial predilection[?]
- Neuroacanthocytosis[?]
- Neuroaxonal dystrophy renal tubular acidosis[?]
- Neuroaxonal dystrophy, late infantile[?]
- Neuroblastoma[?]
- Neurocutaneous melanosis[?]
- Neuroectodermal endocrine syndrome[?]
- Neuroectodermal tumors primitive[?]
- Neuroendocrine cancer[?]
- Neuroendocrine carcinoma of the cervix[?]
- Neuroendocrine tumor[?]
- Neuroepithelioma[?]
- Neurofaciodigitorenal syndrome[?]
- Neurofibrillary tangles[?]
- Neurofibroma[?]
- Neurofibromatosis type 2[?]
- Neurofibromatosis type 3[?]
- Neurofibromatosis type 6[?]
- Neurofibromatosis, familial intestinal[?]
- Neurofibromatosis, Type IV, of Riccardi[?]
- Neurofibromatosis-Noonan syndrome[?]
- Neurofibrosarcoma[?]
- Neurogenic hypertension[?]
- Neuroleptic malignant syndrome
- Neuroma biliary tract[?]
- Neuronal heterotopia[?]
- Neuronal interstitial dysplasia[?]
- Neuronal intestinal pseudoobstruction[?]
- Neuronal intranuclear hyaline inclusion disease[?]
- Neuronal intranuclear inclusion disease[?]
- Neuropathy ataxia and retinis pigmentosa[?]
- Neuropathy congenital sensory neurotrophic keratitis[?]
- Neuropathy hereditary with liability to pressure palsies[?]
- Neuropathy motor sensory type 2 deafness mental retardation[?]
- Neuropathy sensory spastic paraplegia[?]
- Neuropathy, hereditary motor and sensory, LOM type[?]
- Neuropathy, hereditary sensory, type I[?]
- Neuropathy, hereditary sensory, type II[?]
- Neurotoxicity syndromes[?]
- Neutral lipid storage myopathy[?]
- Neutropenia intermittent[?]
- Neutropenia monocytopenia deafness[?]
- Neutropenia, severe chronic[?]
- Nevi flammei, familial multiple[?]
- Nevo syndrome[?]
- Nevoid basal cell carcinoma syndrome[?]
- Nevus of ota retinitis pigmentosa[?]
- Nevus sebaceus of Jadassohn[?]
- Nezelof's syndrome[?]
- Nicolaides Baraitser syndrome[?]
- Niemann-Pick C1 disease[?]
- Niemann-Pick C2 disease[?]
- Niemann-Pick disease type C[?]
- Niemann-Pick disease type D[?]
- Niemann-Pick Disease[?]
- Night blindness skeletal anomalies unusual facies[?]
- Night blindness, congenital stationary[?]
- Nijmegen Breakage Syndrome[?]
- Nivelon Nivelon Mabille syndrome[?]
- Noble Bass Sherman syndrome[?]
- Nocardiosis[?]
- Noise induced deafness[?]
- Noma[?]
- Non functioning pancreatic endocrine tumor[?]
- Nonallergic atopic dermatitis[?]
- Non-Hodgkin lymphoma[?]
- Noninsulin-dependent diabetes mellitus with deafness[?]
- Nonketotic hyperglycinemia[?]
- Non-lissencephalic cortical dysplasia[?]
- Nonmedullary thyroid carcinoma, with cell oxyphilia[?]
- Nonne-Milroy disease[?]
- Non-small cell lung cancer[?]
- Nonsyndromic hereditary hearing impairment[?]
- Noonan like syndrome[?]
- Noonan syndrome[?]
- Norman Roberts lissencephaly syndrome[?]
- Normokalemic periodic paralysis[?]
- Norrie disease[?]
- Northern epilepsy[?]
- Norum disease[?]
- Nose polyposis, familial[?]
- Nosocomephobia[?]
- Nosophobia[?]
- Notalgia paresthetica[?]
- Nova syndrome[?]
- Novak syndrome[?]
- Nuchal bleb, familial[?]
- Nut Hypersensitivity[?]
- Nyctophobia[?]