All diseases

OMIM ID
227330
OMIM term:
FACIODIGITOGENITAL SYNDROME, RECESSIVE
Alternative terms:
AARSKOG-LIKE SYNDROME
KUWAIT TYPE FACIODIGITOGENITAL SYNDROME
(∗) Location:
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/md35acbr