# xeroderma pigmentosum group F

> xeroderma pigmentosum characterized by milder symptoms and later onset of skin cancer that has material basis in homozygous or compound heterozygous mutation in the ERCC4 gene on chromosome 16p13

**Wikidata**: [Q32143775](https://www.wikidata.org/wiki/Q32143775)  
**Source**: https://4ort.xyz/entity/xeroderma-pigmentosum-group-f


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/89544dc5-2d3b-4b7f-b835-3fec714bf7a5--2019-08-14T19:44:06)
5. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_89544dc5-2d3b-4b7f-b835-3fec714bf7a5-2019-08-14T194406.189Z)
6. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000175595/MONDO_0010215)
7. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000175595/Orphanet_276264)
8. [Identifiers.org](https://registry.identifiers.org/registry/doid)