Hyperchloremic metabolic acidosis

Symptom Information:

Symptom ID: HPO:0004918
Synonyms:
Hyperchloremic metabolic acidosis [OMIM:Hyperchloremic metabolic acidosis]
Hyperchloremic metabolic acidosis (HCO3 15.5 +/- 2.0 mM) [OMIM:Hyperchloremic metabolic acidosis (HCO3 15.5 +/- 2.0 mM)]
Hyperchloremic metabolic acidosis (HCO3 17.2 +/- 2.5 mM, dominant) [OMIM:Hyperchloremic metabolic acidosis (HCO3 17.2 +/- 2.5 mM, dominant)]
Hyperchloremic metabolic acidosis (HCO3 17.6 +/- 1.5 mM, recessive) [OMIM:Hyperchloremic metabolic acidosis (HCO3 17.6 +/- 1.5 mM, recessive)]
Quality:
Cross references:
OMIM: "Hyperchloremic metabolic acidosis" [OMIM:Hyperchloremic metabolic acidosis]
OMIM: "Hyperchloremic metabolic acidosis (HCO3 15.5 +/- 2.0 mM)" [OMIM:Hyperchloremic metabolic acidosis (HCO3 15.5 +/- 2.0 mM)]
OMIM: "Hyperchloremic metabolic acidosis (HCO3 17.2 +/- 2.5 mM, dominant)" [OMIM:Hyperchloremic metabolic acidosis (HCO3 17.2 +/- 2.5 mM, dominant)]
OMIM: "Hyperchloremic metabolic acidosis (HCO3 17.6 +/- 1.5 mM, recessive)" [OMIM:Hyperchloremic metabolic acidosis (HCO3 17.6 +/- 1.5 mM, recessive)]
Is a (Direct Parents):
HPO         Hyperchloremic acidosis
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of acid-base homeostasis(HPO:0004360)
             Acidosis(HPO:0001941)
                Hyperchloremic acidosis(HPO:0001995)
                   Hyperchloremic metabolic acidosis(HPO:0004918)
MedDRA:
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

Classic galactosemia (Orphanet:79239)
Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells (Orphanet:83620)
Proximal renal tubular acidosis (Orphanet:47159)
Pseudohypoaldosteronism type 2B (Orphanet:88939)
Pseudohypoaldosteronism type 2D (Orphanet:300525)
Pseudohypoaldosteronism type 2E (Orphanet:300530)