Disease Index
9,486 diseasesnonpapillary renal cell carcinoma
Human disease
nonprogressive cerebellar atxia with mental retardation
Human disease
nonspecific interstitial pneumonia
human disease
nonsyndromic congenital nail disorder 1
Human disease
MeSH: C562907
nonsyndromic congenital nail disorder 10
Human disease
nonsyndromic congenital nail disorder 4
Human disease
MeSH: C536377
nonsyndromic congenital nail disorder 6
Human disease
nonsyndromic congenital nail disorder 7
Human disease
MeSH: C538333
nonsyndromic congenital nail disorder 9
Human disease
nonsyndromic deafness
auditory system disease that is associated with permanent hearing loss caused by damage to structures in the inner ear and/or the middle ear, which is not associated with other signs and symptoms
ICD: H90.5MeSH: C580334
nontuberculous mycobacterial infectious disease
Human disease
MeSH: D009165
Noonan syndrome
congenital, genetically widespread disease considered to be a type of dwarfism affecting boys and girls equally
MeSH: D009634
Noonan syndrome and Noonan-related syndrome
human disease
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
human disease
Noonan syndrome-like disorder with loose anagen hair
normal pressure hydrocephalus
condition in which there is excess cerebrospinal fluid in the ventricles, and with normal or slightly elevated cerebrospinal fluid pressure
MeSH: D006850
Norman–Roberts syndrome
lissencephaly that has_material_basis_in homozygous mutation in the gene encoding reelin (RELN) on chromosome 7q22.
MeSH: C537848
normokalemic periodic paralysis
normophosphatemic familial tumoral calcinosis
calcinosis that is characterized by massive periarticular, and seldom visceral, deposition of calcified tumors
MeSH: C566473
Norrie disease
genetic disorder that primarily affects the eye and almost always leads to blindness
MeSH: C537849
North American Indian childhood cirrhosis
genetic pediatric liver disease
MeSH: C565737
North Carolina macular dystrophy
medical condition
MeSH: C537835
North Sea progressive myoclonus epilepsy
medical condition
Norum disease
disorder of lipoprotein metabolism
MeSH: D007863
nose and cavum anomaly
human disease
NTHL1-related attenuated familial adenomatous polyposis
human disease
nubbin
additional nipple occurring in mammals
ICD: Q83.3
nuclear oculomotor paralysis
human disease
null pituitary adenoma
human disease
null syndrome
The null syndrome is part of the Pelizaeus-Merzbacher disease (PMD; see this term) spectrum and is characterized by mild PMD features associated with demyelinating peripheral neuropathy