GenTIGSA Gene Database on Rare Genetic Disorders
Zimmermann-Laband Syndrome  
Disease Aliases (17)

Fibromatosis, gingival, with abnormal fingers, fingernails, nose, and ears, and splenomegaly

Fibromatosis gingival, hepatosplenomegaly other anomalies

Fibromatosis, gingival, with abnormal fingers, fingernails, nose and ears, and splenomegaly

Gingival fibromatosis - hepatosplenomegaly - other anomalies

Gingival fibromatosis, abnormal fingers, fingernails, nose and ears, and splenomegaly

Gingival fibromatosis-hepatosplenomegaly-other anomalies syndrome

Kcnh1 zimmermann-laband syndrome

Laband-zimmermann syndrome

Zls

Zls1

Zimmerman laband syndrome

Zimmermann-laband syndrome

Zimmermann-laband syndrome 1

Zimmermann-laband syndrome 1; zls1

Zimmermann-laband syndrome caused by mutation in kcnh1

Zimmermann-laband syndrome type 1

Associated Genes (3)
 

NCBI-RefSeq:  ATP6V1B2   (ATPase H+ transporting V1 subunit B2)

External Links:  gnomAD browser   Ensembl   GeneCards

 

NCBI-RefSeq:  KCNH1   (Potassium voltage-gated channel subfamily H member 1)

External Links:  gnomAD browser   Ensembl   GeneCards

 

NCBI-RefSeq:  KCNN3   (Potassium calcium-activated channel subfamily N member 3)

External Links:  gnomAD browser   Ensembl   GeneCards

 


Cross-references of Zimmermann-Laband syndrome OMIM GARD Orphanet NCBI-GTR NCBI-MedGen MalaCards      MeSH Annotations