All diseases

OMIM ID
239300
OMIM term:
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1; HPMRS1
Alternative terms:

(∗) Location:
1p36.11  
(†) Associated OMIM genes:
PIGV  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/j5il6u1s