Coffin-Siris syndrome

Disease Export to PDF
Name:
Coffin-Siris syndrome
Description:
A rare genetic syndromic intellectual disability of broad phenotypic range characterized by developmental delay and variable clinical features which most commonly, but not consistently, include aplasia or hypoplasia of the distal phalanx or nail of the fifth digit, and coarse facial features.
ORPHAcode:
1465
Synonyms:
CSS
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14