Greig cephalopolysyndactyly syndrome
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Greig cephalopolysyndactyly syndrome
Summary
Greig cephalopolysyndactyly syndrome is a developmental defect during embryogenesis[1]. It has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Greig cephalopolysyndactyly syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Greig cephalopolysyndactyly syndrome's instance of is recorded as rare disease[4].
- Greig cephalopolysyndactyly syndrome's instance of is recorded as class of disease[5].
- David Middleton Greig is named after Greig cephalopolysyndactyly syndrome[6].
- Greig cephalopolysyndactyly syndrome is a type of acrocephalosyndactylia[7].
- Greig cephalopolysyndactyly syndrome is a type of syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy[8].
- Greig cephalopolysyndactyly syndrome is a type of genetic disease[9].
- Greig cephalopolysyndactyly syndrome is a type of autosomal dominant disease[10].
- Greig cephalopolysyndactyly syndrome's Commons category is recorded as Greig syndrome[11].
- Greig cephalopolysyndactyly syndrome's NCI Thesaurus ID is recorded as C35255[12].
- Greig cephalopolysyndactyly syndrome's genetic association is recorded as GLI3[13].
- Greig cephalopolysyndactyly syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_14761[14].
- Greig cephalopolysyndactyly syndrome's exact match is recorded as http://identifiers.org/doid/DOID:14761[15].
- Greig cephalopolysyndactyly syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_380[16].
- Greig cephalopolysyndactyly syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
Why It Matters
Greig cephalopolysyndactyly syndrome has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[2] It is known by 10 alternative names across languages and contexts.[18]