Disease #02703 (ACFD (dysplasia, acrocapitofemoral (ACFD)), OMIM:607778)

Official abbreviation ACFD
Name dysplasia, acrocapitofemoral (ACFD)
OMIM ID 607778
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene IHH
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2020-04-03 12:21:03 +02:00 (CEST)

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