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Cantú syndrome

Disease Export to PDF
Name:
Cantú syndrome
Description:
Cantu syndrome is a rare disorder characterized by congenital hypertrichosis, osteochondrodysplasia, cardiomegaly, and dysmorphism.
ORPHAcode:
1517
Synonyms:
Congenital hypertrichosis-acromegaloid facial features spectrum
Congenital hypertrichosis-coarse facial features spectrum
Hypertrichotic osteochondrodysplasia
XREF(s):
Orphanet
OMIM
MeSH
ICD-10
Analyte(s):
ABCC9
KCNJ8
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14