Disease #06515 (SSFSC (Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies), OMIM:617877)

Global Variome shared LOVD

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Official abbreviation	SSFSC
Name	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies
OMIM ID	617877
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	BMP2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-12-10 23:20:41 +01:00 (CET)
Date last edited	N/A

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