Greig cephalopolysyndactyly syndrome
acrocephalosyndactylia that has material basis in mutation in the GLI3 gene which results in abnormal development located in limb, located in head, located in face
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Greig cephalopolysyndactyly syndrome
Summary
Greig cephalopolysyndactyly syndrome is a developmental defect during embryogenesis[1]. It draws 30 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #108 of 308).[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's subclass of is recorded as acrocephalosyndactylia[7].
- Greig cephalopolysyndactyly syndrome's subclass of is recorded as syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy[8].
- Greig cephalopolysyndactyly syndrome's subclass of is recorded as genetic disease[9].
- Greig cephalopolysyndactyly syndrome's subclass of is recorded as autosomal dominant disease[10].
- Greig cephalopolysyndactyly syndrome's Commons category is recorded as Greig syndrome[11].
- Greig cephalopolysyndactyly syndrome's MeSH descriptor ID is recorded as C537300[12].
- Greig cephalopolysyndactyly syndrome's OMIM ID is recorded as 175700[13].
- Greig cephalopolysyndactyly syndrome's ICD-10 ID is recorded as Q87.0[14].
- Greig cephalopolysyndactyly syndrome's DiseasesDB is recorded as 31558[15].
- Greig cephalopolysyndactyly syndrome's KEGG ID is recorded as H02161[16].
- Greig cephalopolysyndactyly syndrome's Disease Ontology ID is recorded as DOID:14761[17].
- Greig cephalopolysyndactyly syndrome's Orphanet ID is recorded as 380[18].
- Greig cephalopolysyndactyly syndrome's NCI Thesaurus ID is recorded as C35255[19].
- Greig cephalopolysyndactyly syndrome's genetic association is recorded as GLI3[20].
- Greig cephalopolysyndactyly syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_14761[21].
- Greig cephalopolysyndactyly syndrome's exact match is recorded as http://identifiers.org/doid/DOID:14761[22].
- Greig cephalopolysyndactyly syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_380[23].
- Greig cephalopolysyndactyly syndrome's UMLS CUI is recorded as C0265306[24].
- Greig cephalopolysyndactyly syndrome's ICD-10-CM is recorded as Q87.0[25].
- Greig cephalopolysyndactyly syndrome's GARD rare disease ID is recorded as 6550[26].
- Greig cephalopolysyndactyly syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[27].
Why It Matters
Greig cephalopolysyndactyly syndrome draws 30 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #108 of 308).[2] It has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[28] It is known by 10 alternative names across languages and contexts.[29]