Weaver syndrome
human disease
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Weaver syndrome
Summary
Weaver syndrome is a developmental defect during embryogenesis[1]. It has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Weaver syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Weaver syndrome's instance of is recorded as designated intractable/rare disease[4].
- Weaver syndrome's instance of is recorded as rare disease[5].
- Weaver syndrome's instance of is recorded as class of disease[6].
- David Weaver is named after Weaver syndrome[7].
- Weaver syndrome is a type of congenital disorder[8].
- Weaver syndrome is a type of overgrowth syndrome[9].
- Weaver syndrome is a type of multiple congenital anomalies/dysmorphic syndrome-intellectual disability[10].
- Weaver syndrome is a type of genetic syndromic intellectual disability[11].
- Weaver syndrome's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4684[12].
- Weaver syndrome's ICD-9-CM is recorded as 759.89[13].
- Weaver syndrome's native label is recorded as {'lang': 'en', 'text': 'Weaver syndrome'}[14].
- Weaver syndrome's NCI Thesaurus ID is recorded as C125599[15].
- Weaver syndrome's health specialty is recorded as medical genetics[16].
- Weaver syndrome's genetic association is recorded as EZH2[17].
- Weaver syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_14731[18].
- Weaver syndrome's exact match is recorded as http://identifiers.org/doid/DOID:14731[19].
- Weaver syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_3447[20].
- Weaver syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[21].
Why It Matters
Weaver syndrome has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.[2] It is known by 7 alternative names across languages and contexts.[22]