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2q37 microdeletion syndrome

The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

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Disease Overview

A chromosomal anomaly involving deletion of chromosome band 2q37 and manifests as three major clinical findings: developmental delay, skeletal malformations and facial dysmorphism.

Synonyms

  • 2q37 deletion syndrome
  • 2q37 microdeletion syndrome
  • 2q37 monosomy
  • Albright hereditary osteodystrophy type 3
  • Albright hereditary osteodystrophy-like syndrome
  • BDMR
  • Del(2)(q37)
  • brachydactyly intellectual disability syndrome
  • brachydactyly mental retardation syndrome
  • brachydactyly-intellectual disability syndrome
  • brachydactyly-mental retardation syndrome
  • chromosome 2q37 deletion syndrome
  • deletion 2q37
  • deletion 2q37-qter
  • monosomy 2q37-qter2q37 deletion syndrome
  • 2q37 microdeletion syndrome
  • 2q37 monosomy
  • Albright hereditary osteodystrophy type 3
  • Albright hereditary osteodystrophy-like syndrome
  • BDMR
  • Del(2)(q37)
  • brachydactyly intellectual disability syndrome
  • brachydactyly mental retardation syndrome
  • brachydactyly-intellectual disability syndrome
  • brachydactyly-mental retardation syndrome
  • chromosome 2q37 deletion syndrome
  • deletion 2q37
  • deletion 2q37-qter
  • monosomy 2q37-qter
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