Cytoscape Web
Click node...


11 OMIM references -
12 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
3 associated genes
4 signs/symptoms
MODY syndrome
Well-differentiated liposarcoma

ABCC8 CDK4
BLK HMGA2
CEL MDM2
GCK
HNF1A
HNF4A
INS
KCNJ11
KLF11
NEUROD1
PAX4
PDX1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
HNF4A
(0.63)
MDM2



Citations in the biomedical literature:


MODY syndrome
ABCC8 BLK CEL GCK HNF1A HNF4A
INS KCNJ11 KLF11 NEUROD1 PAX4 PDX1

Well-differentiated liposarcoma
CDK4 HMGA2 MDM2



MODY syndrome
Well-differentiated liposarcoma

Synonym(s):
- Maturity-onset diabetes of the young

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

Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
Classification (Orphanet):
- Rare oncologic disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
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:
11 OMIM references -
No MeSH references
External references:
No OMIM references
No MeSH references

Well-differentiated liposarcoma

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


MODY syndrome

(no data available)