Hyperglycinuria

Symptom Information:

Symptom ID: HPO:0003108
Synonyms:
Glycinuria [HPO:0003108]
Glycinuria [OMIM:Glycinuria]
Hyperglycinuria [OMIM:Hyperglycinuria]
Quality:
Cross references:
OMIM: "Glycinuria" [OMIM:Glycinuria]
OMIM: "Hyperglycinuria" [OMIM:Hyperglycinuria]
UMLS:C1853747 "Hyperglycinuria" [HPO:0003108]
Is a (Direct Parents):
HPO         Abnormality of glycine metabolism
HPO         Aminoaciduria
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of urine homeostasis(HPO:0003110)
             Aciduria(HPO:0012072)
                Aminoaciduria(HPO:0003355)
                   Hyperglycinuria(HPO:0003108)
          Abnormality of carboxylic acid metabolism(HPO:0004354)
             Abnormality of amino acid metabolism(HPO:0004337)
                Aminoaciduria(HPO:0003355)
                   Hyperglycinuria(HPO:0003108)
                Abnormality of serine family amino acid metabolism(HPO:0010894)
                   Abnormality of glycine metabolism(HPO:0010895)
                      Hyperglycinuria(HPO:0003108)
       Abnormality of the genitourinary system(HPO:0000119)
          Abnormality of the urinary system(HPO:0000079)
             Abnormality of the urinary system physiology(HPO:0011277)
                Abnormality of urine homeostasis(HPO:0003110)
                   Aciduria(HPO:0012072)
                      Aminoaciduria(HPO:0003355)
                         Hyperglycinuria(HPO:0003108)
MedDRA:
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

3-@METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY (OMIM:210210)
GLUCOGLYCINURIA (OMIM:138070)
Glycine encephalopathy (Orphanet:407)
HYPERGLYCINURIA (OMIM:138500)
Hyperprolinemia type 1 (Orphanet:419)
Hyperprolinemia type 2 (Orphanet:79101)
INDOLYLACROYL GLYCINURIA WITH MENTAL RETARDATION (OMIM:243050)
Iminoglycinuria (Orphanet:42062)
Isovaleric acidemia (Orphanet:33)
Medium chain acyl-CoA dehydrogenase deficiency (Orphanet:42)
Propionic acidemia (Orphanet:35)