Disease #01034 (Fibular hypoplasia and complex brachydactyly, OMIM:228900)

Official abbreviation -
Name Fibular hypoplasia and complex brachydactyly
OMIM ID 228900
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene GDF5
Associated tissues -
Disease features -
Remarks -

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