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3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
9 signs/symptoms
Dedifferentiated liposarcoma
Oculopharyngeal muscular dystrophy

CDK4 PABPN1
HMGA2
MDM2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
MDM2
(0.63)
PABPN1



Citations in the biomedical literature:


Dedifferentiated liposarcoma
CDK4 HMGA2 MDM2
Oculopharyngeal muscular dystrophy
PABPN1



Dedifferentiated liposarcoma
Oculopharyngeal muscular dystrophy

Synonym(s):
- DDLS

Synonym(s):
- OPMD

Classification (Orphanet):
- Rare oncologic disease
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: adult
Type of inheritance: sporadic
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant

External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D039141

Oculopharyngeal muscular dystrophy

Very frequent
- Abnormal muscle biopsy / muscle enzymes / CPK / LDH / aldolase / creatin phosphokinase
- Anomaly of the pharynx / pharyngeal anomaly
- Autosomal dominant inheritance
- Autosomal recessive inheritance
- Muscle hypotrophy / atrophy / dystrophy / agenesis / amyotrophy
- Myopathy
- Ophthalmoplegia / ophthalmoparesis / oculomotor palsy
- Ptosis

Occasional
- Expressionless face / amimia


Dedifferentiated liposarcoma

(no data available)