Disease #05829 (RCDP5 (chondrodysplasia punctata, rhizomelic, type 5 (RCDP5)), OMIM:616716)

Official abbreviation RCDP5
Name chondrodysplasia punctata, rhizomelic, type 5 (RCDP5)
OMIM ID 616716
Human Phenotype Ontology Project (HPO) HPO
Inheritance AR
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene PEX5
Associated tissues -
Disease features -
Remarks -

  Powered by LOVD v.3.0 Build 25
LOVD software ©2004-2020 Leiden University Medical Center 		There are currently no updates.