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Zimmermann-Laband syndrome

Disease Export to PDF
Name:
Zimmermann-Laband syndrome
Description:
A rare genetic multiple congenital anomalies syndrome characterized by gingival fibromatosis, coarse facial appearance, and absence or hypoplasia of nails or terminal phalanges of hands and feet.
ORPHAcode:
3473
Synonyms:
Gingival fibromatosis-hepatosplenomegaly-other anomalies syndrome
Laband syndrome
XREF(s):
Orphanet
ICD-10
OMIM
OMIM
OMIM
OMIM
Analyte(s):
KCNN3
ATP6V1B2
KCNH1
KCNMA1
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14