Pendred syndrome
genetic disorder
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Pendred syndrome
Summary
Pendred syndrome is a head and neck disease[1]. It has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Pendred syndrome's instance of is recorded as head and neck disease[3].
- Pendred syndrome's instance of is recorded as developmental defect during embryogenesis[4].
- Pendred syndrome's instance of is recorded as rare disease[5].
- Pendred syndrome's instance of is recorded as class of disease[6].
- Pendred syndrome is a type of autosomal recessive disease[7].
- Pendred syndrome is a type of syndromic genetic deafness[8].
- Pendred syndrome is a type of syndromic hypothyroidism[9].
- Pendred syndrome is a type of Thyroid dyshormonogenesis[10].
- Pendred syndrome is a type of syndrome[11].
- Pendred syndrome is a type of congenital hypothyroidism[12].
- Pendred syndrome's NCI Thesaurus ID is recorded as C121745[13].
- Pendred syndrome's health specialty is recorded as endocrinology[14].
- Pendred syndrome's genetic association is recorded as SLC26A4[15].
- Pendred syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060744[16].
- Pendred syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060744[17].
- Pendred syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_705[18].
- Pendred syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[19].
Why It Matters
Pendred syndrome has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.[2] It is known by 17 alternative names across languages and contexts.[20]