All diseases

OMIM ID
257200
OMIM term:
NIEMANN-PICK DISEASE, TYPE A
Alternative terms:
SPHINGOMYELIN LIPIDOSIS
SPHINGOMYELINASE DEFICIENCY NIEMANN-PICK DISEASE, INTERMEDIATE, PROTRACTED NEUROVISCERAL, INCLUDED
(∗) Location:
11p15.4  
(†) Associated OMIM genes:
SMPD1  
(‡) Associated MGI genes:
Smpd1  

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