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4 OMIM references -
2 associated genes
1 sign/symptom
PROTEIN INTERACTIONS: 1
3 associated genes
4 signs/symptoms
Familial hypospadias
Well-differentiated liposarcoma

AR CDK4
MAMLD1 HMGA2
MDM2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
AR
(0.96)
MDM2



Citations in the biomedical literature:


Familial hypospadias
AR MAMLD1
Well-differentiated liposarcoma
CDK4 HMGA2 MDM2



Familial hypospadias
Well-differentiated liposarcoma

Synonym(s):
(no synonyms)

Synonym(s):
- ALT
- Atypical lipoma
- Atypical lipomatous tumor
- WDLS

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare urogenital disease
Classification (Orphanet):
- Rare oncologic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal dominant
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:
No OMIM references
No MeSH references

Familial hypospadias
Well-differentiated liposarcoma

Very frequent
- Hypospadias / epispadias / bent penis



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

Occasional
- Functional anomalies of the kidney and the urinary tract
- Intestinal transit disorder