Disease Browser
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Parent Node: Hypercholesterolemia (D006937) | Parent Node: Hypertension (D006973) | Parent Node: Renal Tubular Transport, Inborn Errors (D015499) | ..Starting node ..Hypomagnesemia, Hypertension, and Hypercholesterolemia, Mitochondrial (C564024)
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Sister Nodes: | ..Acidosis, Renal Tubular (D000141) 11
| ..Azotemia, Familial (C566233)
| ..Bartter Syndrome (D001477) 8
| ..Dent Disease (D057973) 1
| ..Donnai-Barrow syndrome (C536390)
| ..Fanconi Syndrome (D005198) 3
| ..Gitelman Syndrome (D053579) 1
| ..Glycosuria, Renal (D006030) 1
| ..Hypomagnesemia 1, Intestinal (C566593)
| ..Hypomagnesemia 2, renal (C537152)
| ..Hypomagnesemia 4, Renal (C567127)
| ..Hypomagnesemia 5, Renal, with Ocular Involvement (C565423)
| ..Hypomagnesemia primary (C537153)
| ..Hypomagnesemia, Hypertension, and Hypercholesterolemia, Mitochondrial (C564024)
| ..Hypophosphatemia, Familial (D007015) 11
| ..Hypouricemia, Familial Renal, due to Tubular Hypersecretion (C564405)
| ..Hypouricemia, Hypercalcinuria, and Decreased Bone Density (C565475)
| ..Hypouricemia, Renal, 2 (C567426)
| ..Iminoglycinuria (C536285)
| ..Liddle Syndrome (D056929)
| ..Nephrolithiasis-Osteoporosis, Hypophosphatemic, 1 (C567363)
| ..Nephrolithiasis-Osteoporosis, Hypophosphatemic, 2 (C567362)
| ..Oculocerebrorenal Syndrome (D009800) 1
| ..Pseudohypoaldosteronism (D011546) 4
| ..Renal Aminoacidurias (D000608) 9
| ..Renal hypouricemia (C537757)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 5585 |
Name: | Hypomagnesemia, Hypertension, and Hypercholesterolemia, Mitochondrial |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D006937|MESH:D006973|MESH:D015499 |
TreeNumbers: | C12.777.419.815/C564024 |C13.351.968.419.815/C564024 |C14.907.489/C564024 |C16.320.565.861/C564024 |C18.452.584.500.500.396/C564024 |C18.452.648.861/C564024 |
Synonyms: | |
Slim Mappings: | Cardiovascular disease|Genetic disease (inborn)|Metabolic disease|Urogenital disease (female)|Urogenital disease (male) |
Reference: |
MedGen: C564024
MeSH: C564024
OMIM:
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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