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Alveolar rhabdomyosarcoma
1 OMIM reference -
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal recessive limb-girdle muscular dystrophy type 2G
1 OMIM reference -
1 associated gene
No signs/symptoms info
Alveolar rhabdomyosarcoma
Autosomal recessive limb-girdle muscular dystrophy type 2G

FOXO1
(UniProt - OMIM)
 TCAP
(UniProt - OMIM)
PAX3
(UniProt - OMIM)
PAX7
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
PAX7
(0.63)
TCAP


Citations in the biomedical literature:


Alveolar rhabdomyosarcoma
FOXO1 PAX3 PAX7
Autosomal recessive limb-girdle muscular dystrophy type 2G
TCAP



Alveolar rhabdomyosarcoma
Autosomal recessive limb-girdle muscular dystrophy type 2G

Synonym(s):
(no synonyms)

Synonym(s):
- LGMD2G
- Limb girdle muscular dystrophy due to telethonin deficiency
Classification (Orphanet):
- Rare oncologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: no data available
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
1 MeSH reference: D018232
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.