Generalized aminoaciduria

Symptom Information:

Symptom ID: HPO:0002909
Synonyms:
Generalized nonspecific aminoaciduria [HPO:0002909]
Generalized aminoaciduria [OMIM:Generalized aminoaciduria]
Generalized nonspecific aminoaciduria [OMIM:Generalized nonspecific aminoaciduria]
Aminoaciduria, generalized [OMIM:Aminoaciduria, generalized]
Quality:
Cross references:
OMIM: "Generalized aminoaciduria" [OMIM:Generalized aminoaciduria]
OMIM: "Generalized nonspecific aminoaciduria" [OMIM:Generalized nonspecific aminoaciduria]
OMIM: "Aminoaciduria, generalized" [OMIM:Aminoaciduria, generalized]
Is a (Direct Parents):
HPO         Aminoaciduria
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)
                   Aciduria(HPO:0012072)
                      Aminoaciduria(HPO:0003355)
                         Generalized aminoaciduria(HPO:0002909)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of urine homeostasis(HPO:0003110)
             Aciduria(HPO:0012072)
                Aminoaciduria(HPO:0003355)
                   Generalized aminoaciduria(HPO:0002909)
          Abnormality of carboxylic acid metabolism(HPO:0004354)
             Abnormality of amino acid metabolism(HPO:0004337)
                Aminoaciduria(HPO:0003355)
                   Generalized aminoaciduria(HPO:0002909)
MedDRA:
Database Frequency: 13 / 7739
Resource:

All diseases associated with this symptom:

Arthrogryposis - renal dysfunction - cholestasis (Orphanet:2697)
BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY (OMIM:210550)
CYSTINOSIS, NEPHROPATHIC (OMIM:219800)
FANCONI RENOTUBULAR SYNDROME 2 (OMIM:613388)
FANCONI RENOTUBULAR SYNDROME 3 (OMIM:615605)
Glycogen storage disease due to GLUT2 deficiency (Orphanet:2088)
HOMOZYGOUS 11p15-p14 DELETION SYNDROME (OMIM:606528)
Hypocalcemic vitamin D-dependent rickets (Orphanet:289157)
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency (Orphanet:279934)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
North Carolina macular dystrophy (Orphanet:75327)
Primary Fanconi syndrome (Orphanet:3337)
VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A (OMIM:264700)