Hyperpigmentation of the skin

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Hyperpigmentation of the skin

ORPHA:79375Category

What it is

Orphanet has not published a description for this disease yet. The identifiers, classification and cross-references below are still current.

Key facts

Classified as
Category

Genes reported in subtypes

ABCB6ACDADARBRCA1BRCA2BRIP1COQ6CTC1DKC1ERCC4FAAP100FANCAFANCBFANCCFANCD2FANCEFANCFFANCGFANCIFANCLFANCMGNASGRHL2KITLGKRT14KRT5LZTR1MAD2L2MAP2K2MYH8MYO5ANF1NF2NHP2NOP10NPM1PALB2PARNPDE11APOFUT1POGLUT1PRKAR1APSENENRAD51RAD51CRFWD3RMI2RTEL1SASH1SLC29A3SLX4SMARCB1SPRED1TERCTERTTINF2TOP3ATYMSUBE2TUSB1WRAP53XRCC2

Orphanet records these genes on 20 more specific entries under this disorder, not on this entry itself:

A well-studied disease is usually split into subtypes, and the gene is curated on whichever one the evidence belongs to. Open a subtype to see which gene goes with it.

Cross-references

MEDDRA 10040865MESH D017495MONDO 0019289MONDO 19289UMLS C0162834

Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.

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