22q13 deletion syndrome
human disease
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22q13 deletion syndrome
Summary
22q13 deletion syndrome is a developmental defect during embryogenesis[1]. It draws 92 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #76 of 308).[2]
Key Facts
- 22q13 deletion syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- 22q13 deletion syndrome's instance of is recorded as rare disease[4].
- 22q13 deletion syndrome's instance of is recorded as class of disease[5].
- Katy Phelan is named after 22q13 deletion syndrome[6].
- Joann M. McDermid is named after 22q13 deletion syndrome[7].
- 22q13 deletion syndrome's subclass of is recorded as partial deletion of the long arm of chromosome 22[8].
- 22q13 deletion syndrome's subclass of is recorded as genetic syndromic intellectual disability[9].
- 22q13 deletion syndrome's subclass of is recorded as chromosomal deletion syndrome[10].
- 22q13 deletion syndrome's subclass of is recorded as disease[11].
- 22q13 deletion syndrome's MeSH descriptor ID is recorded as C536801[12].
- 22q13 deletion syndrome's OMIM ID is recorded as 606232[13].
- 22q13 deletion syndrome's ICD-10 ID is recorded as Q93[14].
- 22q13 deletion syndrome's DiseasesDB is recorded as 34793[15].
- 22q13 deletion syndrome's Freebase ID is recorded as /m/0fnvc2[16].
- 22q13 deletion syndrome's KEGG ID is recorded as H01238[17].
- 22q13 deletion syndrome's ICPC 2 ID is recorded as A90[18].
- 22q13 deletion syndrome's Disease Ontology ID is recorded as DOID:0080354[19].
- 22q13 deletion syndrome's Orphanet ID is recorded as 48652[20].
- 22q13 deletion syndrome's ICD-9-CM is recorded as 758.39[21].
- 22q13 deletion syndrome's NCI Thesaurus ID is recorded as C157124[22].
- 22q13 deletion syndrome's health specialty is recorded as genetics[23].
- 22q13 deletion syndrome's genetic association is recorded as SHANK3[24].
- 22q13 deletion syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0080354[25].
- 22q13 deletion syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080354[26].
- 22q13 deletion syndrome's UMLS CUI is recorded as C2931332[27].
Why It Matters
22q13 deletion syndrome draws 92 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #76 of 308).[2] It has Wikipedia articles in 12 language editions, a strong signal of global cultural recognition.[28] It is known by 12 alternative names across languages and contexts.[29]