List of diseases (N): Difference between revisions
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Latest revision as of 16:57, 9 August 2012
N-Nas
- 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
- Naxos disease
Ne
Nec-Neo
- Necrotizing encephalopathy, infantile subacute
- Necrotizing fasciitis
- Negative rheumatoid factor polyarthritis
- Neisseria meningitidis
- Nelson syndrome
- Nemaline myopathy
- Nemaline Myopathy, Amish Type
- Neonatal hemochromatosis
- Neonatal hepatitis
- Neonatal herpes
- Neonatal ovarian cyst
- Neonatal transient jaundice
Nep-Net
- 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
- Nephrotic syndrome ocular anomalies
- Nephrotic syndrome, idiopathic, steroid-resistant
- Nerve sheath neoplasm
- Nesidioblastosis of pancreas
- Netherton syndrome ichthyosis
Neu
Neuh
Neur
Neura-Neuri
- 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
Neuro
Neuroa-Neurog
- 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
- Neurofibromatosis type 2
- Neurofibromatosis type 3
- Neurofibromatosis type 6
- Neurofibromatosis, familial intestinal
- Neurofibromatosis, Type IV, of Riccardi
- Neurofibromatosis-Noonan syndrome
- Neurofibrosarcoma
- Neurogenic hypertension
Neurol-Neurot
- 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
Neut
- Neutral lipid storage myopathy
- Neutropenia intermittent
- Neutropenia monocytopenia deafness
- Neutropenia, severe chronic
Nev-Nez
- Nevi flammei, familial multiple
- Nevo syndrome
- Nevoid basal cell carcinoma syndrome
- Nevus of ota retinitis pigmentosa
- Nevus sebaceus of Jadassohn
- Nezelof's syndrome
Ni
- 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
No
Nob-Nor
- Noble Bass Sherman syndrome
- Nocardiosis
- Noise induced deafness
- Noma
- Non-24-hour sleep-wake disorder
- 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