C173103Level 7
Trichothiodystrophy 2, Photosensitive
**Semantic type:** Disease or Syndrome
**Definition:** An autosomal recessive subtype of trichothiodystrophy caused by mutation(s) in the ERCC3 gene, encoding general transcription and DNA repair factor IIH helicase subunit XPB.
**Synonyms:** - TTD2
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