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

Global Variome shared LOVD

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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	-
Phenotype entries for this disease	-
Associated with 1 gene	PEX5
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-09-07 10:40:32 +02:00 (CEST)
Date last edited	N/A

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