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Xeroderma pigmentosum complementation group C
1 OMIM reference -
1 associated gene
39 connected diseases
No signs/symptoms info
Disease Type of connection
B-cell chronic lymphocytic leukemia
Xeroderma pigmentosum complementation group E
Xeroderma pigmentosum complementation group B
Apolipoprotein A-I deficiency
Ataxia-telangiectasia variant
Combined cervical dystonia
Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome
Mantle cell lymphoma
Seckel syndrome
Tangier disease
Atypical teratoid tumor
Coffin-Siris syndrome
Familial multiple meningioma
Familial rhabdoid tumor
Neurofibromatosis type 3
Xeroderma pigmentosum complementation group A
Dedifferentiated liposarcoma
Well-differentiated liposarcoma
Adrenocortical carcinoma
Essential thrombocythemia
Familial pancreatic carcinoma
Giant cell glioblastoma
Li-Fraumeni syndrome
Nestor-Guillermo progeria syndrome
Papilloma of choroid plexus
Precursor B-cell acute lymphoblastic leukemia
Cockayne syndrome type 1
Fanconi anemia
Xeroderma pigmentosum complementation group F
Atypical Rett syndrome
Dyskeratosis congenita
Intellectual deficit, X-linked - psychosis - macroorchidism
Rett syndrome
Severe neonatal-onset encephalopathy with microcephaly
Trisomy Xq28
X-linked non-syndromic intellectual deficit

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

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

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references

Gene symbol UniProt reference OMIM reference
XPC Q01831613208
No signs/symptoms info available.