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 Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene PEX5
Associated tissues -
Disease features -
Remarks -

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