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Autosomal dominant Emery-Dreifuss muscular dystrophy
4 OMIM references -
4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Myxoid/round cell liposarcoma
1 OMIM reference -
2 associated genes
4 signs/symptoms
Autosomal dominant Emery-Dreifuss muscular dystrophy
Myxoid/round cell liposarcoma

LMNA
(UniProt - OMIM)
 DDIT3
(UniProt - OMIM)
SYNE1
(UniProt - OMIM)
 FUS
(UniProt - OMIM)
SYNE2
(UniProt - OMIM)
TMEM43
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
LMNA
(0.49)
FUS


Citations in the biomedical literature:


Autosomal dominant Emery-Dreifuss muscular dystrophy
LMNA SYNE1 SYNE2 TMEM43
Myxoid/round cell liposarcoma
DDIT3 FUS



Autosomal dominant Emery-Dreifuss muscular dystrophy
Myxoid/round cell liposarcoma

Synonym(s):
(no synonyms)

Synonym(s):
- MRCLS
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare oncologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Neoplasms -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: adult
Type of inheritance: sporadic
External references:
4 OMIM references -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D018208
Myxoid/round cell liposarcoma

Very frequent
- Soft tissue sarcoma / cancer / tumor / liposarcoma / myosarcoma
- Subcutaneous nodules / lipomas / tumefaction / swelling

Occasional
- Acute abdominal pain / colic
- Intestinal transit disorder


Autosomal dominant Emery-Dreifuss muscular dystrophy

(no data available)