All diseases

OMIM ID
257220
OMIM term:
NIEMANN-PICK DISEASE, TYPE C1; NPC1
Alternative terms:
NIEMANN-PICK DISEASE, TYPE C; NPC
NIEMANN-PICK DISEASE WITH CHOLESTEROL ESTERIFICATION BLOCK
NIEMANN-PICK DISEASE, SUBACUTE JUVENILE FORM
NIEMANN-PICK DISEASE, CHRONIC NEURONOPATHIC FORM
NIEMANN-PICK DISEASE WITHOUT SPHINGOMYELINASE DEFICIENCY
NEUROVISCERAL STORAGE DISEASE WITH VERTICAL SUPRANUCLEAR OPHTHALMOPLEGIA NIEMANN-PICK DISEASE, TYPE D, INCLUDED
NIEMANN-PICK DISEASE, NOVA SCOTIAN TYPE, INCLUDED
(∗) Location:
18q11.2  
(†) Associated OMIM genes:
NPC1  
(‡) Associated MGI genes:
Npc1   Npc2  

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