2q37 monosomy
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2q37 monosomy
Summary
2q37 monosomy is a developmental defect during embryogenesis[1]. It draws 2 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #134 of 308).[2]
Key Facts
- 2q37 monosomy's image is recorded as Chromosome 2.svg[3].
- 2q37 monosomy's instance of is recorded as developmental defect during embryogenesis[4].
- 2q37 monosomy's instance of is recorded as class of disease[5].
- 2q37 monosomy's subclass of is recorded as chromosomal deletion syndrome[6].
- 2q37 monosomy's subclass of is recorded as genetic syndromic intellectual disability[7].
- 2q37 monosomy's subclass of is recorded as syndrome with brachydactyly[8].
- 2q37 monosomy's subclass of is recorded as chromosome 2q deletion[9].
- 2q37 monosomy's subclass of is recorded as 2q37 deletion syndrome[10].
- 2q37 monosomy's MeSH descriptor ID is recorded as C538317[11].
- 2q37 monosomy's OMIM ID is recorded as 600430[12].
- 2q37 monosomy's Freebase ID is recorded as /m/0dddxvx[13].
- 2q37 monosomy's Orphanet ID is recorded as 1001[14].
- 2q37 monosomy's ICD-9-CM is recorded as 758.39[15].
- 2q37 monosomy's NCI Thesaurus ID is recorded as C129021[16].
- 2q37 monosomy's health specialty is recorded as medical genetics[17].
- 2q37 monosomy's genetic association is recorded as HDAC4[18].
- 2q37 monosomy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1001[19].
- 2q37 monosomy's UMLS CUI is recorded as C1838126[20].
- 2q37 monosomy's UMLS CUI is recorded as C2931817[21].
- 2q37 monosomy's ICD-10-CM is recorded as Q93.5[22].
- 2q37 monosomy's GARD rare disease ID is recorded as 10202[23].
- 2q37 monosomy's Mondo ID is recorded as MONDO_0010886[24].
- 2q37 monosomy's Microsoft Academic ID is recorded as 2777775661[25].
- 2q37 monosomy's ICD-11 ID is recorded as 1167208445[26].
Why It Matters
2q37 monosomy draws 2 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #134 of 308).[2] It is known by 13 alternative names across languages and contexts.[27]