Robinow Syndrome, Autosomal Recessive 2 (RRS2)

Alias:

Rrs2

Robinow, Autosomal Recessive Syndrome, Type 2

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Robinow Syndrome, Autosomal Recessive 2, also known as rrs2, is related to catastrophic antiphospholipid syndrome and cryopyrin-associated periodic syndrome. An important gene associated with Robinow Syndrome, Autosomal Recessive 2 is NXN (Nucleoredoxin). Related phenotypes are gingival overgrowth and hypertelorism

Related ID：

MALACARDS：RBN023

OMIM：618529

MESH：D004392