All diseases

OMIM ID
235000
OMIM term:
HEMIHYPERPLASIA, ISOLATED; IH
Alternative terms:
HEMIHYPERPLASIA; HHP
HEMIHYPERTROPHY, ISOLATED HEMI-3 SYNDROME, INCLUDED
(∗) Location:
11p15  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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