22q13 deletion syndrome
human disease
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22q13 deletion syndrome
Summary
22q13 deletion syndrome is a developmental defect during embryogenesis[1]. It has Wikipedia articles in 12 language editions, a strong signal of global cultural recognition.[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 is a type of partial deletion of the long arm of chromosome 22[8].
- 22q13 deletion syndrome is a type of genetic syndromic intellectual disability[9].
- 22q13 deletion syndrome is a type of chromosomal deletion syndrome[10].
- 22q13 deletion syndrome is a type of disease[11].
- 22q13 deletion syndrome's ICPC 2 ID is recorded as A90[12].
- 22q13 deletion syndrome's ICD-9-CM is recorded as 758.39[13].
- 22q13 deletion syndrome's NCI Thesaurus ID is recorded as C157124[14].
- 22q13 deletion syndrome's health specialty is recorded as genetics[15].
- 22q13 deletion syndrome's genetic association is recorded as SHANK3[16].
- 22q13 deletion syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0080354[17].
- 22q13 deletion syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080354[18].
- 22q13 deletion syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[19].
Why It Matters
22q13 deletion syndrome has Wikipedia articles in 12 language editions, a strong signal of global cultural recognition.[2] It is known by 12 alternative names across languages and contexts.[20]