trichothiodystrophy 3, photosensitive
human disease
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trichothiodystrophy 3, photosensitive
Summary
trichothiodystrophy 3, photosensitive is a developmental defect during embryogenesis[1].
Key Facts
- trichothiodystrophy 3, photosensitive's instance of is recorded as developmental defect during embryogenesis[2].
- trichothiodystrophy 3, photosensitive's instance of is recorded as class of disease[3].
- trichothiodystrophy 3, photosensitive's subclass of is recorded as trichothiodystrophy syndromes[4].
- trichothiodystrophy 3, photosensitive's subclass of is recorded as autosomal recessive disease[5].
- trichothiodystrophy 3, photosensitive's OMIM ID is recorded as 616395[6].
- trichothiodystrophy 3, photosensitive's Disease Ontology ID is recorded as DOID:0111871[7].
- trichothiodystrophy 3, photosensitive's NCI Thesaurus ID is recorded as C173099[8].
- trichothiodystrophy 3, photosensitive's genetic association is recorded as GTF2H5[9].
- trichothiodystrophy 3, photosensitive's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111871[10].
- trichothiodystrophy 3, photosensitive's exact match is recorded as http://identifiers.org/doid/DOID:0111871[11].
- trichothiodystrophy 3, photosensitive's UMLS CUI is recorded as C4017171[12].
- trichothiodystrophy 3, photosensitive's Mondo ID is recorded as MONDO_0014619[13].
- trichothiodystrophy 3, photosensitive's UniProt disease ID is recorded as DI-04434[14].