Disease #00376 (SRTD5 (dysplasia, short-rib thoracic, type 5, with/without polydactyly (SRTD-5)), OMIM:614376)

Official abbreviation	SRTD5
Name	dysplasia, short-rib thoracic, type 5, with/without polydactyly (SRTD-5)
OMIM ID	614376
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	WDR19
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-05-02 09:59:17 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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Global Variome shared LOVD