Zimmermann-Laband Syndrome 1 (ZLS1)

Alias:

Zimmermann-Laband Syndrome

Laband Syndrome

Fibromatosis, Gingival, with Abnormal Fingers, Fingernails, Nose, and Ears, and Splenomegaly

Gingival Fibromatosis-Hepatosplenomegaly-Other Anomalies Syndrome

Zls1

Gingival Fibromatosis, Abnormal Fingers, Fingernails, Nose and Ears and Splenomegaly

Zimmermann-Laband Syndrome, Type 1

Zimmermann Laband Syndrome

Zimmerman Laband Syndrome

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Zimmermann-Laband Syndrome 1, also known as zimmermann-laband syndrome, is related to hypertrichosis and gingival hypertrophy, and has symptoms including seizures An important gene associated with Zimmermann-Laband Syndrome 1 is KCNH1 (Potassium Voltage-Gated Channel Subfamily H Member 1), and among its related pathways/superpathways are Transmission across Chemical Synapses and Potassium Channels. Affiliated tissues include skin, and related phenotypes are gingival fibromatosis and intellectual disability

Related ID：

MALACARDS：ZMM002

OMIM：135500

MESH：D000015