U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Mowat-Wilson syndrome due to monosomy 2q22

MedGen UID:
1723926
•Concept ID:
C5437617
•
Disease or Syndrome
Synonyms: Hirschsprung disease and intellectual disability due to 2q22 microdeletion; Hirschsprung disease and intellectual disability due to del(2)(q22); Hirschsprung disease and intellectual disability due to monosomy 2q22; Mowat-Wilson syndrome due to 2q22 microdeletion; Mowat-Wilson syndrome due to del(2)q(22); Mowat-Wilson syndrome due to monosomy type 2q22
SNOMED CT: Hirschsprung disease and intellectual disability due to del(2)(q22) (890118006); Hirschsprung disease and intellectual disability due to monosomy 2q22 (890118006); Hirschsprung disease and intellectual disability due to 2q22 microdeletion (890118006); Mowat-Wilson syndrome due to del(2)q(22) (890118006); Mowat-Wilson syndrome due to monosomy 2q22 (890118006); Mowat-Wilson syndrome due to 2q22 microdeletion (890118006)
 
Monarch Initiative: MONDO:0016855
Orphanet: ORPHA261537

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVMowat-Wilson syndrome due to monosomy 2q22

Supplemental Content

Table of contents

    Clinical resources

    Reviews

    Related information

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...