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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
4 associated genes
No signs/symptoms info
Atypical Mayer-Rokitansky-Küster-Hauser syndrome
Squamous cell carcinoma of head and neck

WNT4 ING1
ING3
PTEN
TNFRSF10B


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
WNT4
(0.63)
PTEN



Citations in the biomedical literature:


Atypical Mayer-Rokitansky-Küster-Hauser syndrome
WNT4
Squamous cell carcinoma of head and neck
ING1 ING3 PTEN TNFRSF10B



Atypical Mayer-Rokitansky-Küster-Hauser syndrome
Squamous cell carcinoma of head and neck

Synonym(s):
- Atypical MRKH syndrome
- Atypical Rokitansky syndrome
- WNT4 deficiency

Synonym(s):
- HNSCC
- Head and neck squamous cell carcinoma

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare endocrine disease
- Rare genetic disease
- Rare gynecologic or obstetric disease
- Rare infertility
- Rare renal disease
- Rare urogenital disease
Classification (Orphanet):
- Rare oncologic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)

External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: C535575

No signs/symptoms info available.