Disease #07203 (SSFSC2 (short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies, type 2), OMIM:619184)

Global Variome shared LOVD

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Official abbreviation	SSFSC2
Name	short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies, type 2
OMIM ID	619184
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SCUBE3
Associated tissues	-
Disease features	-
Remarks	-
Date created	2025-11-21 19:15:27 +01:00 (CET)
Date last edited	N/A

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