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3 associated genes
4 signs/symptoms
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
4 signs/symptoms
Well-differentiated liposarcoma
HSD10 disease, atypical type

CDK4 HSD17B10
HMGA2
MDM2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
MDM2
(0.63)
HSD17B10



Citations in the biomedical literature:


Well-differentiated liposarcoma
CDK4 HMGA2 MDM2
HSD10 disease, atypical type
HSD17B10



Well-differentiated liposarcoma
HSD10 disease, atypical type

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

Synonym(s):
- HSD10 deficiency, atypical type
- Syndromic X-linked intellectual disability type 10
- X-linked intellectual disability-choreoathetosis-abnormal behavior syndrome

Classification (Orphanet):
- Rare oncologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
(no data available)

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 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: x-linked recessive

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

Well-differentiated liposarcoma
HSD10 disease, atypical type

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


Very frequent
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Movement disorder
- Psychic / behavioural troubles
- X-linked recessive inheritance