trichothiodystrophy 2, photosensitive
human disease
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trichothiodystrophy 2, photosensitive
Summary
trichothiodystrophy 2, photosensitive is a developmental defect during embryogenesis[1].
Key Facts
- trichothiodystrophy 2, photosensitive's instance of is recorded as developmental defect during embryogenesis[2].
- trichothiodystrophy 2, photosensitive's instance of is recorded as class of disease[3].
- trichothiodystrophy 2, photosensitive's subclass of is recorded as trichothiodystrophy syndromes[4].
- trichothiodystrophy 2, photosensitive's subclass of is recorded as autosomal recessive disease[5].
- trichothiodystrophy 2, photosensitive's OMIM ID is recorded as 616390[6].
- trichothiodystrophy 2, photosensitive's Disease Ontology ID is recorded as DOID:0111869[7].
- trichothiodystrophy 2, photosensitive's NCI Thesaurus ID is recorded as C173103[8].
- trichothiodystrophy 2, photosensitive's genetic association is recorded as ERCC3[9].
- trichothiodystrophy 2, photosensitive's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111869[10].
- trichothiodystrophy 2, photosensitive's exact match is recorded as http://identifiers.org/doid/DOID:0111869[11].
- trichothiodystrophy 2, photosensitive's UMLS CUI is recorded as C4225344[12].
- trichothiodystrophy 2, photosensitive's Mondo ID is recorded as MONDO_0014615[13].
- trichothiodystrophy 2, photosensitive's UniProt disease ID is recorded as DI-04433[14].