All diseases

OMIM ID
241500
OMIM term:
HYPOPHOSPHATASIA, INFANTILE
Alternative terms:
HOPS
PHOSPHOETHANOLAMINURIA HYPOPHOSPHATASIA, PERINATAL LETHAL, INCLUDED
(∗) Location:
1p36.12  
(†) Associated OMIM genes:
ALPL  
(‡) Associated MGI genes:
Alpl  

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