Treacher Collins syndrome
human genetic disorder
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Treacher Collins syndrome
Summary
Treacher Collins syndrome is a rare disease[1]. It has Wikipedia articles in 27 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Treacher Collins syndrome's instance of is recorded as rare disease[3].
- Treacher Collins syndrome's instance of is recorded as class of disease[4].
- Edward Treacher Collins is named after Treacher Collins syndrome[5].
- Treacher Collins syndrome is a type of autosomal dominant disease[6].
- Treacher Collins syndrome is a type of first arch syndrome[7].
- Treacher Collins syndrome is a type of syndrome[8].
- Treacher Collins syndrome is a type of disease[9].
- Treacher Collins syndrome's Commons category is recorded as Treacher Collins syndrome[10].
- Treacher Collins syndrome's NCI Thesaurus ID is recorded as C75018[11].
- Treacher Collins syndrome's health specialty is recorded as medical genetics[12].
- Treacher Collins syndrome's genetic association is recorded as TCOF1[13].
- Treacher Collins syndrome's genetic association is recorded as POLR1D[14].
- Treacher Collins syndrome's genetic association is recorded as POLR1C[15].
- Treacher Collins syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_2908[16].
- Treacher Collins syndrome's exact match is recorded as http://identifiers.org/doid/DOID:2908[17].
- Treacher Collins syndrome's exact match is recorded as http://purl.obolibrary.org/obo/HP_0005321[18].
- Treacher Collins syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_861[19].
- Treacher Collins syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[20].
Why It Matters
Treacher Collins syndrome has Wikipedia articles in 27 language editions, a strong signal of global cultural recognition.[2] It is known by 8 alternative names across languages and contexts.[21]