Disease #05367 (SMDCF (dysplasia, spondylometaphyseal, corner fracture type (SMDCF)), OMIM:184255)

Official abbreviation	SMDCF
Name	dysplasia, spondylometaphyseal, corner fracture type (SMDCF)
OMIM ID	184255
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	FN1
Associated tissues	-
Disease features	autosomal dominant
Remarks	-
Date created	2017-12-29 15:32:31 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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Global Variome shared LOVD