Hyperglycinemia

Symptom Information:

Symptom ID: HPO:0002154
Synonyms:
Hyperglycinaemia [HPO:0002154]
Hyperglycinemia [OMIM:Hyperglycinemia]
Hyperglycinemia (1 patient) [OMIM:Hyperglycinemia (1 patient)]
Quality:
Cross references:
OMIM: "Hyperglycinemia" [OMIM:Hyperglycinemia]
OMIM: "Hyperglycinemia (1 patient)" [OMIM:Hyperglycinemia (1 patient)]
UMLS:C0268559 "Hyperglycinaemia" [HPO:0002154]
Is a (Direct Parents):
HPO         Abnormality of serum amino acid levels
HPO         Abnormality of glycine metabolism
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)
                   Hyperglycinemia(HPO:0002154)
                Abnormality of serine family amino acid metabolism(HPO:0010894)
                   Abnormality of glycine metabolism(HPO:0010895)
                      Hyperglycinemia(HPO:0002154)
MedDRA:
Database Frequency: 12 / 7739
Resource:

All diseases associated with this symptom:

Argininosuccinic aciduria (Orphanet:23)
D-glyceric aciduria (Orphanet:941)
Glycine encephalopathy (Orphanet:407)
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency (Orphanet:279934)
Propionic acidemia (Orphanet:35)
Pyruvate dehydrogenase lipoic acid synthetase deficiency (OMIM:614462)
Vitamin B12-responsive methylmalonic acidemia (Orphanet:28)
Vitamin B12-responsive methylmalonic acidemia type cblA (Orphanet:79310)
Vitamin B12-responsive methylmalonic acidemia type cblB (Orphanet:79311)
Vitamin B12-unresponsive methylmalonic acidemia (Orphanet:27)
Vitamin B12-unresponsive methylmalonic acidemia type mut- (Orphanet:79312)
Vitamin B12-unresponsive methylmalonic acidemia type mut0 (Orphanet:289916)