Disease Browser
Parent Node: cerebral lipidosis with dementia (MONDO:0020143) Parent Node: monogenic disease with epilepsy (MONDO:0015653) Parent Node: Niemann-Pick disease (MONDO:0001982) Parent Node: secondary interstitial lung disease in childhood and adulthood associated with a metabolic disease (MONDO:0017037) Parent Node: sphingolipidosis with epilepsy (MONDO:0018299) Parent Node: supranuclear oculomotor palsy (MONDO:0020257) Parent Node: unclassified primitive or secondary maculopathy (MONDO:0020244) ..Starting node .. Niemann-Pick disease type C () Child Nodes:
........Niemann-Pick disease type C, adult neurologic onset () ........Niemann-Pick disease type C, juvenile neurologic onset () ........Niemann-Pick disease type C, late infantile neurologic onset () ........Niemann-Pick disease type C, severe early infantile neurologic onset () ........Niemann-Pick disease type C, severe perinatal form () ........Niemann-Pick disease, type C1 () ........Niemann-Pick disease, type C2 () Sister Nodes: ..autosomal dominant osteopetrosis 2 () ..Bardet-Biedl syndrome () ..cone-rod dystrophy () ..congenital hypotrichosis with juvenile macular dystrophy () ..cystoid macular edema () ..enhanced S-cone syndrome () ..Farber lipogranulomatosis () ..foveal hypoplasia-presenile cataract syndrome () ..galactosialidosis () ..GM1 gangliosidosis () ..Hermansky-Pudlak syndrome 2 () ..infantile Refsum disease () ..Krabbe disease () ..Laurence-Moon syndrome () ..Leigh disease () ..metachromatic leukodystrophy () ..mucolipidosis type IV () ..neuronal ceroid lipofuscinosis () ..Niemann-Pick disease type C () ..Rubinstein-Taybi syndrome () ..Sjogren-Larsson syndrome () ..Sorsby's fundus dystrophy () ..X-linked retinoschisis () ..Zellweger syndrome () MONDO is developed by the Monarch Initiative . Human Disease MESH is developed by UMLS . Further data from MedGen , OMIM ,ClinVar , CTD