Tryptophanuria

Symptom Information:

Symptom ID: HPO:0003361
Synonyms:
Tryptophanuria [OMIM:Tryptophanuria]
Quality:
Cross references:
OMIM: "Tryptophanuria" [OMIM:Tryptophanuria]
UMLS:C0268472 "Tryptophanuria" [HPO:0003361]
Is a (Direct Parents):
HPO         Aminoaciduria
HPO         Abnormality of tryptophan 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)
                Aminoaciduria(HPO:0003355)
                   Tryptophanuria(HPO:0003361)
                Abnormality of aromatic amino acid family metabolism(HPO:0004338)
                   Abnormality of tryptophan metabolism(HPO:0004365)
                      Tryptophanuria(HPO:0003361)
          Abnormality of urine homeostasis(HPO:0003110)
             Aciduria(HPO:0012072)
                Aminoaciduria(HPO:0003355)
                   Tryptophanuria(HPO:0003361)
       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)
                         Tryptophanuria(HPO:0003361)
MedDRA:
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

Blue diaper syndrome (Orphanet:94086)
Hypertryptophanemia (Orphanet:2224)
TRYPTOPHANURIA WITH DWARFISM (OMIM:276100)