Waardenburg's syndrome
genetic condition involving hearing loss and depigmentation
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Waardenburg's syndrome
Summary
Waardenburg's syndrome is a rare disease[1]. It has Wikipedia articles in 20 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Waardenburg's syndrome's instance of is recorded as rare disease[3].
- Waardenburg's syndrome's instance of is recorded as class of disease[4].
- Petrus Johannes Waardenburg is named after Waardenburg's syndrome[5].
- Waardenburg's syndrome is a type of genetic deafness[6].
- Waardenburg's syndrome is a type of autosomal dominant disease[7].
- Waardenburg's syndrome is a type of syndrome[8].
- Waardenburg's syndrome is a type of disease[9].
- Waardenburg's syndrome's Commons category is recorded as Waardenburg syndrome[10].
- Waardenburg's syndrome's NCI Thesaurus ID is recorded as C85222[11].
- Waardenburg's syndrome's health specialty is recorded as medical genetics[12].
- Waardenburg's syndrome's genetic association is recorded as EDNRB[13].
- Waardenburg's syndrome's genetic association is recorded as PAX3[14].
- Waardenburg's syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_9258[15].
- Waardenburg's syndrome's exact match is recorded as http://identifiers.org/doid/DOID:9258[16].
- Waardenburg's syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_3440[17].
- Waardenburg's syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[18].
- Waardenburg's syndrome's comorbidity is recorded as premature greying of hair[19].
Why It Matters
Waardenburg's syndrome has Wikipedia articles in 20 language editions, a strong signal of global cultural recognition.[2] It is known by 30 alternative names across languages and contexts.[20]