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 -

  Powered by LOVD v.3.0 Build 27
LOVD software ©2004-2021 Leiden University Medical Center 		There are currently no updates.