Hyperlysinemia
Symptom Information:
Symptom ID: | HPO:0002161 | ||||
Synonyms: |
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Quality: | |||||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of metabolism/homeostasis(HPO:0001939) Abnormality of carboxylic acid metabolism(HPO:0004354) Abnormality of amino acid metabolism(HPO:0004337) Abnormality of serum amino acid levels(HPO:0003112) Hyperlysinemia(HPO:0002161) Abnormality of aspartate family amino acid metabolism(HPO:0010899) Abnormality of lysine metabolism(HPO:0010908) Hyperlysinemia(HPO:0002161) MedDRA: |
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Database Frequency: | 7 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
2,4-@DIENOYL-CoA REDUCTASE 1, MITOCHONDRIAL | (OMIM:222745) |
2,4-@DIENOYL-CoA REDUCTASE DEFICIENCY | (OMIM:616034) |
HYPERLYSINURIA WITH HYPERAMMONEMIA | (OMIM:238750) |
Hyperlysinemia due to defect in lysine transport into mitochondria | (OMIM:238710) |
Hyperlysinemia, type I | (OMIM:238700) |
Pyruvate carboxylase deficiency | (Orphanet:3008) |
Saccharopinuria | (Orphanet:3124) |