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4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
1 OMIM reference -
1 associated gene
No signs/symptoms info
Trichothiodystrophy
Adrenocortical carcinoma

ERCC2 TP53
ERCC3
GTF2H5
MPLKIP


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ERCC3
ERCC2
(0.89)
(0.88)
TP53
TP53



Citations in the biomedical literature:


Trichothiodystrophy
ERCC2 ERCC3 GTF2H5 MPLKIP
Adrenocortical carcinoma
TP53



Trichothiodystrophy
Adrenocortical carcinoma

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare infertility
- Rare skin disease
Classification (Orphanet):
- Rare circulatory system disease
- Rare endocrine disease
- Rare infertility
- Rare oncologic disease
- Rare renal disease

Classification (ICD10):
- Diseases of the skin and subcutaneous tissue -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: sporadic

External references:
No OMIM references
2 MeSH references: C536559 / D054463
External references:
1 OMIM reference -
1 MeSH reference: D018268

No signs/symptoms info available.