Hypomethioninemia

Symptom Information:

Symptom ID: HPO:0003658
Synonyms:
Decreased plasma methionine [HPO:0003658]
Decreased serum methionine [HPO:0003658]
Decreased serum methionine [OMIM:Decreased serum methionine]
Hypomethioninemia [OMIM:Hypomethioninemia]
Quality:
Cross references:
OMIM: "Decreased serum methionine" [OMIM:Decreased serum methionine]
OMIM: "Hypomethioninemia" [OMIM:Hypomethioninemia]
Is a (Direct Parents):
HPO         Abnormality of methionine 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 sulfur amino acid metabolism(HPO:0004339)
                   Abnormality of methionine metabolism(HPO:0010901)
                      Hypomethioninemia(HPO:0003658)
                Abnormality of serum amino acid levels(HPO:0003112)
                   Hypomethioninemia(HPO:0003658)
                Abnormality of aspartate family amino acid metabolism(HPO:0010899)
                   Abnormality of methionine metabolism(HPO:0010901)
                      Hypomethioninemia(HPO:0003658)
MedDRA:
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

Methylcobalamin deficiency type cblDv1 (Orphanet:308380)
Methylcobalamin deficiency type cblE (Orphanet:2169)
Methylcobalamin deficiency type cblG (Orphanet:2170)
Methylmalonic acidemia with homocystinuria, type cblC (Orphanet:79282)
Methylmalonic acidemia with homocystinuria, type cblD (Orphanet:79283)
Vitamin B12-responsive methylmalonic acidemia, type cblDv2 (Orphanet:308442)