Hyperlysinemia

Symptom Information:

Symptom ID: HPO:0002161
Synonyms:
Hyperlysinaemia [HPO:0002161]
Hyperlysinemia [OMIM:Hyperlysinemia]
Quality:
Cross references:
OMIM: "Hyperlysinemia" [OMIM:Hyperlysinemia]
UMLS:C0268553 "Hyperlysinaemia" [HPO:0002161]
Is a (Direct Parents):
HPO         Abnormality of lysine metabolism
HPO         Abnormality of serum amino acid levels
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:
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)