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Hereditary Spherocytosis Type 5 (MONDO:0012985)

Any hereditary spherocytosis in which the cause of the disease is a mutation in the EPB42 gene.

Overview

Category

Ontology ID

Internal:14025

Synonyms

EPB42 hereditary spherocytosis

HS5

SPH5

hereditary spherocytosis caused by mutation in EPB42

hereditary spherocytosis type 5

spherocytosis, hereditary, 5

spherocytosis, type 5

Mapped terms

DOID:0110920

GARD:0015578

MEDGEN:436371

MESH:C567202

OMIM:612690

UMLS:C2675192

Child terms

Unknown children.