MONDO:0011702

Ontologies▸mondo▸classes▸MONDO:0011702

dilated cardiomyopathy 1L

http://purl.obolibrary.org/obo/MONDO_0011702

Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the SGCD gene.

Also appears inpride efo

Exact Synonyms

cardiomyopathy, dilated, type 1L

CMD1L

dilated cardiomyopathy type 1L

familial isolated dilated cardiomyopathy caused by mutation in SGCD

SGCD familial isolated dilated cardiomyopathy

Related Synonyms

cardiomyopathy, dilated, 1L

Exact matchInclude obsolete termsInclude imported terms

disease (25,660)
- human disease (22,700)
  - cardiovascular disorder (1,609)
    - heart disorder (716)
      - cardiogenetic disease (443)
        familial cardiomyopathy (228)
        familial dilated cardiomyopathy (85)
        familial isolated dilated cardiomyopathy (45)
        dilated cardiomyopathy 1L
      - cardiomyopathy (283)
        familial cardiomyopathy (228)
        familial dilated cardiomyopathy (85)
        familial isolated dilated cardiomyopathy (45)
        dilated cardiomyopathy 1L
        intrinsic cardiomyopathy (261)
        dilated cardiomyopathy (90)
        familial dilated cardiomyopathy (85)
        familial isolated dilated cardiomyopathy (45)
        dilated cardiomyopathy 1L
  - hereditary disease (11,467)
    - cardiogenetic disease (443)
      - familial cardiomyopathy (228)
        familial dilated cardiomyopathy (85)
        familial isolated dilated cardiomyopathy (45)
        dilated cardiomyopathy 1L
    - hereditary neurological disease (3,438)
      - qualitative or quantitative defects of delta-sarcoglycan (2)
        dilated cardiomyopathy 1L
  - musculoskeletal system disorder (3,118)
    - muscle tissue disorder (912)
      - cardiomyopathy (283)
        familial cardiomyopathy (228)
        familial dilated cardiomyopathy (85)
        familial isolated dilated cardiomyopathy (45)
        dilated cardiomyopathy 1L
        intrinsic cardiomyopathy (261)
        dilated cardiomyopathy (90)
        familial dilated cardiomyopathy (85)
        familial isolated dilated cardiomyopathy (45)
        dilated cardiomyopathy 1L
  - nervous system disorder (5,563)
    - hereditary neurological disease (3,438)
      - qualitative or quantitative defects of delta-sarcoglycan (2)
        dilated cardiomyopathy 1L
    - qualitative or quantitative protein defects in neuromuscular diseases (132)
      - sarcoglycanopathy (9)
        qualitative or quantitative defects of delta-sarcoglycan (2)
        dilated cardiomyopathy 1L

class Information

has exact match

has_dbxref

in_subset

term tracker item

https://github.com/monarch-initiative/mondo/issues/7693

class Relations

Subclass of