FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term metal metabolism disorder ID (Ontology) DOID:896 (Human Disease)
Definition An inherited metabolic disorder that involves metabolic disturbances in the processing or distribution of dietary minerals.
Also Known As "inborn metal metabolism disorder"
Comment
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DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
Records annotated with this exact term (annotations to child terms are NOT included)
Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS      15
Human Disease Models (FBhh)  DOID       2
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Alleles Genes Human Disease Models
 metal metabolism disorder      15      8      2
 ameliorates | metal metabolism disorder       3       --       --
 model of | metal metabolism disorder      12       --       --
Spanning Tree (Parents/Children)
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disease of metabolism__
genetic disease________|
                       inherited metabolic disorder
                        |__metal metabolism disorder  64 rec.
                            |__acrodermatitis enteropathica 1 rec.
                            |__atransferrinemia 2 rec.
                            |__autosomal dominant hypocalcemia 1 rec.
                            |   |__autosomal dominant hypocalcemia 1
                            |   |__autosomal dominant hypocalcemia 2 1 rec.
                            |__familial periodic paralysis 2 rec.
                            |   |__hyperkalemic periodic paralysis 1 rec.
                            |   |__hypokalemic periodic paralysis 2 rec.
                            |__hemochromatosis 4 rec.
                            |   |__African iron overload
                            |   |__hemochromatosis type 1 1 rec.
                            |   |__hemochromatosis type 2(+)
                            |   |__hemochromatosis type 3
                            |   |__hemochromatosis type 4
                            |   |__hemochromatosis type 5 3 rec.
                            |__hypermanganesemia with dystonia 2 rec.
                            |   |__hypermanganesemia with dystonia 1 1 rec.
                            |   |__hypermanganesemia with dystonia 2 1 rec.
                            |__Menkes disease 15 rec.
                            |__molybdenum cofactor deficiency 4 rec.
                            |   |__molybdenum cofactor deficiency type A 1 rec.
                            |   |__molybdenum cofactor deficiency type B 2 rec.
                            |   |__molybdenum cofactor deficiency type C 1 rec.
                            |__occipital horn syndrome 2 rec.
                            |__primary hypomagnesemia 4 rec.
                            |   |__intestinal hypomagnesemia 1 1 rec.
                            |   |__renal hypomagnesemia 2
                            |   |__renal hypomagnesemia 3
                            |   |__renal hypomagnesemia 4 1 rec.
                            |   |__renal hypomagnesemia 5 with ocular involvement
                            |   |__renal hypomagnesemia 6 1 rec.
                            |   |__renal hypomagnesemia 7, with or without dilated cardiomyopathy 1 rec.
                            |__pseudohypoparathyroidism 3 rec.
                            |   |__pseudohypoparathyroidism type 1A 2 rec.
                            |   |__pseudohypoparathyroidism type 1B 3 rec.
                            |   |__pseudohypoparathyroidism type 1C 2 rec.
                            |   |__pseudopseudohypoparathyroidism 2 rec.
                            |__Wilson disease 4 rec.
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Is a inherited metabolic disorder
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Synonyms
  • "inborn metal metabolism disorder" EXACT
Secondary IDs
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MESH:D008664
UMLS_CUI:C0025534