Disease Index
9,486 diseasesNiemann-Pick disease type C, severe early infantile neurologic onset
human disease
Niemann-Pick disease type C, severe perinatal form
human disease
Niemann-Pick disease type E
Niemann-Pick disease, type E is a poorly defined adult-onset and non-neuronopathic form of Niemann-Pick disease
Niemann–Pick disease, type C
autosomal recessive lipid storage disorder that is characterized by accumulation of cholesterol and sphingomyelins in cells of the viscera and the central nervous system
ICD: E75.2MeSH: D052556
night blindness-skeletal anomalies-dysmorphism syndrome
This syndrome is characterized by night blindness, skeletal abnormalities (sloping shoulders, joint hyperextensibility, minor radiological anomalies) and characteristic facies (periorbital anomalies, malar flatness, retrognathia)
Nijmegen breakage syndrome
human disease
MeSH: D049932
Nijmegen breakage syndrome-like disorder
human disease
MeSH: C567767
NIK deficiency
immunodeficiency disorder caused by loss of function mutation in NIK (MAP3K14)
Nipah virus infection
disease caused by Nipah virus
NK-cell enteropathy
medical condition
nocardiosis
infectious disease affecting either the lungs (pulmonary nocardiosis) or the whole body (systemic nocardiosis)
MeSH: D009617
nodal marginal zone B cell lymphoma
marginal zone B-cell lymphoma which morphologically resembles lymph nodes involved by marginal zone lymphomas of extranodal or splenic types, but without evidence of extranodal or splenic disease
nodular cutaneous amyloidosis
Nodular lichen myxedematosus
medical condition
Nodular lymphocyte predominant Hodgkin's lymphoma
medical condition
ICD: C81.0
nodular medulloblastoma
Human disease
nodular neuronal heterotopia
human disease
nodular nonsuppurative panniculitis
cutaneous condition characterized by recurrent subcutaneous nodules that heal with depression of the overlying skin
MeSH: D010201
Nodular regenerative hyperplasia
medical condition
nodular urticaria pigmentosa
human disease
noma
gangrenous infection of the mouth and face
MeSH: D009625
non progressive epilepsy and/or ataxia with myoclonus as a major feature
human disease
non-24-hour sleep-wake disorder
term
ICD: G47.2
non-acquired combined pituitary hormone deficiencies without extra-pituitary malformations
human disease
non-acquired pituitary hormone deficiency
human disease
non-acquired premature ovarian failure
human disease
non-amyloid monoclonal immunoglobulin deposition disease
human disease
non-central nervous system-localized embryonal carcinoma
human disease
non-classic congenital lipoid adrenal hyperplasia due to STAR deficiency
human disease
non-distal monosomy 10q
human disease