Trimethylaminuria

Symptom Information:

Symptom ID: HPO:0003614
Synonyms:
Trimethylaminuria [OMIM:Trimethylaminuria]
Trimethylaminuria [MedDRA:10068233]
Quality:
Cross references:
OMIM: "Trimethylaminuria" [OMIM:Trimethylaminuria]
UMLS:C0342739 "Trimethylaminuria" [HPO:0003614]
Is a (Direct Parents):
HPO         Abnormality of urine homeostasis
MedDRA Inborn errors of metabolism NEC
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       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)
                   Trimethylaminuria(HPO:0003614)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of urine homeostasis(HPO:0003110)
             Trimethylaminuria(HPO:0003614)
MedDRA:
Congenital, familial and genetic disorders(MedDRA:10010331)
    Metabolic and nutritional disorders congenital(MedDRA:10027424)
       Inborn errors of metabolism NEC(MedDRA:10021606)
          Trimethylaminuria(HPO:0003614)
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

TRIMETHYLAMINURIA (OMIM:602079)