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Microtriplication 11q24.1

MedGen UID:
1656562
Concept ID:
C4749373
Disease or Syndrome
Synonyms: microtriplication 11q24.1; Tetrasomy 11q24.1; tetrasomy 11q24.1
SNOMED CT: Microtriplication 11q24.1 (770663003); Tetrasomy 11q24.1 (770663003)
 
Monarch Initiative: MONDO:0017335
Orphanet: ORPHA289522

Definition

An extremely rare partial autosomal tetrasomy, resulting from a partial triplication of the long arm of chromosome 11, with characteristics of intellectual disability (with severe verbal impairment), short stature with small extremities, keratoconus and distinctive facial features (round, course face, upward slanting palpebral fissures, mild synophrys, large nose with thick ala nasi and triangular tip, large mouth with broad lips, short and smooth philtrum, large protruded chin, ears with adherent lobules). [from SNOMEDCT_US]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVMicrotriplication 11q24.1

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