Xeroderma pigmentosum complementation group D |
Familial hypospadias |
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INTERACTOME ASSOCIATIONS (click on a score value to see the evidence) |
ERCC2
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| AR
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Citations in the biomedical literature:
Xeroderma pigmentosum complementation group D |
Familial hypospadias |
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Synonym(s): - XPD
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Synonym(s): (no synonyms) |
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Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic disease - Rare neurologic disease - Rare oncologic disease - Rare otorhinolaryngologic disease - Rare skin disease
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Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare urogenital disease
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Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -
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Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -
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Epidemiological data: Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal recessive
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Epidemiological data: Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal dominant
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External references: 1 OMIM reference -
No MeSH references | |
External references: 4 OMIM references - No MeSH references
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Familial hypospadias |
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Very frequent - Hypospadias / epispadias / bent penis
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Xeroderma pigmentosum complementation group D |
(no data available)
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