Disease #06967 (MYODRIF (myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facie), OMIM:618975)

Official abbreviation	MYODRIF
Name	myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facie
OMIM ID	618975
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MYOD1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-09-27 08:09:41 +02:00 (CEST)
Date last edited	N/A

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Global Variome shared LOVD