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Disease association ontology term - MONDO:0016354 - xeroderma pigmentosum-Cockayne syndrome complex

Term summary

ID
MONDO:0016354
Name
xeroderma pigmentosum-Cockayne syndrome complex
Ontology or CV name
Disease association
Definition
Xeroderma pigmentosum/Cockayne syndrome complex (XP/CS complex) is characterized by the cutaneous features of xeroderma pigmentosum (XP) together with the systemic and neurological features of Cockayne syndrome (CS).

Parents

Annotation

Disease association

MONDO:0012531 - xeroderma pigmentosum group B

References:

Genes:

MONDO:0010212 - xeroderma pigmentosum group D

References:

Genes:

MONDO:0010215 - xeroderma pigmentosum group F

References:

Genes:

MONDO:0010216 - xeroderma pigmentosum group G

References:

Genes: