Acromesomelic Dysplasia

Alias:

Acromesomelic Dysplasia Hunter-Thompson Type

Dysplasia, Acromesomelic

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Acromesomelic Dysplasia, also known as dysplasia, acromesomelic, is related to acromesomelic dysplasia 2a and acromesomelic dysplasia 2c. An important gene associated with Acromesomelic Dysplasia is NPR2 (Natriuretic Peptide Receptor 2), and among its related pathways/superpathways are Phospholipase-C Pathway and Extracellular matrix organization. Affiliated tissues include bone and kidney, and related phenotypes are Decreased substrate adherent cell growth and Increased human cytomegalovirus (HCMV) strain AD169 replication

Related ID：

MALACARDS：ACR016

MESH：C535658