Disease #04279 (SCDO5 (dysostosis, spondylocostal, autosomal recessive, type 5 (SCDO-5)), OMIM:122600)

Global Variome shared LOVD

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Official abbreviation	SCDO5
Name	dysostosis, spondylocostal, autosomal recessive, type 5 (SCDO-5)
OMIM ID	122600
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant, Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TBX6
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-05-29 16:26:21 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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