2q37 monosomy
Deletion 2q37 or monosomy 2q37 is a chromosomal anomaly involving deletion of chromosome band 2q37 and manifests as three major clinical findings: developmental delay, skeletal malformations and facial dysmorphism
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2q37 monosomy
Summary
2q37 monosomy is a developmental defect during embryogenesis[1]. It draws 13 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #134 of 308).[2]
Key Facts
- 2q37 monosomy's instance of is recorded as developmental defect during embryogenesis[3].
- 2q37 monosomy's instance of is recorded as class of disease[4].
- 2q37 monosomy is a type of chromosomal deletion syndrome[5].
- 2q37 monosomy is a type of genetic syndromic intellectual disability[6].
- 2q37 monosomy is a type of syndrome with brachydactyly[7].
- 2q37 monosomy is a type of chromosome 2q deletion[8].
- 2q37 monosomy is a type of 2q37 deletion syndrome[9].
- 2q37 monosomy's ICD-9-CM is recorded as 758.39[10].
- 2q37 monosomy's NCI Thesaurus ID is recorded as C129021[11].
- 2q37 monosomy's health specialty is recorded as medical genetics[12].
- 2q37 monosomy's genetic association is recorded as HDAC4[13].
- 2q37 monosomy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1001[14].
Why It Matters
2q37 monosomy draws 13 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.[15]