Disease #00133 (MFM9 (MYOPATHY, MYOFIBRILLAR, 9, WITH EARLY RESPIRATORY FAILURE), OMIM:603689)

Official abbreviation	MFM9
Name	MYOPATHY, MYOFIBRILLAR, 9, WITH EARLY RESPIRATORY FAILURE
OMIM ID	603689
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TTN
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-06-16 10:21:03 +00:00 (UTC)
Date last edited	N/A

MVZ für Humangenetik Regensburg