1. Diseases
  2. Wolf-Hirschhorn syndrome

Wolf-Hirschhorn syndrome

Disease Export to PDF
Name:
Wolf-Hirschhorn syndrome
Description:
A developmental disorder characterized by typical craniofacial features, prenatal and postnatal growth impairment, intellectual disability, severe delayed psychomotor development, seizures, and hypotonia.
ORPHAcode:
280
Synonyms:
4p- syndrome
Distal deletion 4p
Distal monosomy 4p
Telomeric deletion 4p
XREF(s):
Orphanet
MeSH
MeSH
OMIM
MedDRA
ICD-10
Analyte(s):
PIGG
CPLX1
CTBP1
NSD2
NELFA
LETM1
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14