Disease #06618 (BDA1D (Brachydactyly, type A1, D), OMIM:616849)

Official abbreviation BDA1D
Name Brachydactyly, type A1, D
OMIM ID 616849
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene BMPR1B
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A

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