Disease #00722 (MMFD (macrocephaly, macrosomia, facial dysmorphism syndrome (MMFD)), OMIM:614192)

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Official abbreviation	MMFD
Name	macrocephaly, macrosomia, facial dysmorphism syndrome (MMFD)
OMIM ID	614192
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	RNF135
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A