Disease #05875 (SRTD19 (dysplasia, thoracic, short-rib, type 19 with/without polydactyly (SRTD19)), OMIM:617895)

Global Variome shared LOVD

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Official abbreviation	SRTD19
Name	dysplasia, thoracic, short-rib, type 19 with/without polydactyly (SRTD19)
OMIM ID	617895
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	IFT81
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-11-11 09:42:18 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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