Renal Fanconi syndrome

Symptom Information:

Symptom ID: HPO:0001994
Synonyms:
'de toni-fanconi-debre' syndrome [HPO:0001994]
Renal tubular fanconi syndrome [HPO:0001994]
'De Toni-Fanconi-Debre' syndrome [OMIM:'De Toni-Fanconi-Debre' syndrome]
Renal tubular Fanconi syndrome [OMIM:Renal tubular Fanconi syndrome]
Quality:
Cross references:
OMIM: "'De Toni-Fanconi-Debre' syndrome" [OMIM:'De Toni-Fanconi-Debre' syndrome]
OMIM: "Renal tubular Fanconi syndrome" [OMIM:Renal tubular Fanconi syndrome]
Is a (Direct Parents):
HPO         Abnormality of renal resorption
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)
                Abnormal renal physiology(HPO:0012211)
                   Abnormality of renal resorption(HPO:0011038)
                      Renal Fanconi syndrome(HPO:0001994)
             Abnormality of the upper urinary tract(HPO:0010935)
                Abnormality of the kidney(HPO:0000077)
                   Abnormal renal physiology(HPO:0012211)
                      Abnormality of renal resorption(HPO:0011038)
                         Renal Fanconi syndrome(HPO:0001994)
MedDRA:
Database Frequency: 12 / 7739
Resource:

All diseases associated with this symptom:

Arthrogryposis - renal dysfunction - cholestasis (Orphanet:2697)
CYSTINOSIS, NEPHROPATHIC (OMIM:219800)
Cystinosis (Orphanet:213)
Dent disease type 1 (Orphanet:93622)
Fanconi syndrome - ichthyosis - dysmorphism (Orphanet:1981)
Isolated cytochrome C oxidase deficiency (Orphanet:254905)
Kearns-Sayre syndrome (Orphanet:480)
Leigh syndrome (Orphanet:506)
MELAS (Orphanet:550)
Oculocerebrorenal syndrome (Orphanet:534)
Pearson syndrome (Orphanet:699)
Tyrosinemia type 1 (Orphanet:882)