Disease #05757 (SFMMP (split-foot malformation with mesoaxial polydactyly (SFMMP)), OMIM:616890)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	SFMMP
Name	split-foot malformation with mesoaxial polydactyly (SFMMP)
OMIM ID	616890
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MAP3K20
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-05-25 13:40:12 +02:00 (CEST)
Date last edited	2020-05-25 13:40:30 +02:00 (CEST)

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