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Disease association ontology term - MONDO:0004689 - inborn metal metabolism disorder

Term summary

ID
MONDO:0004689
Name
inborn metal metabolism disorder
Ontology or CV name
Disease association
Definition
An inherited metabolic disorder that involves metabolic disturbances in the processing or distribution of dietary minerals.

Parents

Annotation

Disease association

MONDO:0011417 - hemochromatosis type 3

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Genes:

MONDO:0859328 - hypomagnesemia 7, renal, with or without dilated cardiomyopathy

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Genes:

MONDO:0010651 - Menkes disease

References:

Genes:

MONDO:0011301 - pseudohypoparathyroidism type 1B

References:

Genes:

MONDO:0980701 - sulfite oxidase deficiency due to molybdenum cofactor deficiency type B2

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Genes:

MONDO:0010200 - Wilson disease

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Genes: