DisGeNET - a database of gene-disease associations

Source: ORPHANET

Diseases associated to the Gene: MYPN ×

Results per page

Gene

Disease

Variant

Source

Semantic type

Disease Class

Type

HPO Term

DO Class

CUI	Disease	Type	Disease Class	Semantic type	DO Class	HPO Term	Num. genes
C0340427	Familial dilated cardiomyopathy	disease	Cardiovascular Diseases	Disease or Syndrome	genetic disease; disease of anatomical entity		44
C0546125	Nemaline Myopathy, Childhood Onset	disease	Musculoskeletal Diseases; Nervous System Diseases	Disease or Syndrome			7
C0348616	Other restrictive cardiomyopathy	disease	Cardiovascular Diseases	Disease or Syndrome	disease of anatomical entity		5
C3710589	Cap Myopathy	disease	Musculoskeletal Diseases; Nervous System Diseases	Disease or Syndrome; Congenital Abnormality			3