Hyperchloremia

Symptom Information:

Symptom ID: HPO:0011423
Synonyms:
Hyperchloremia (mean 109 mM) [OMIM:Hyperchloremia (mean 109 mM)]
Hyperchloremia (mean 111 mM) [OMIM:Hyperchloremia (mean 111 mM)]
Hyperchloremia (mean 114 mM) [OMIM:Hyperchloremia (mean 114 mM)]
Hyperchloremia (mean >110 mM in both dominant and recessive) [OMIM:Hyperchloremia (mean >110 mM in both dominant and recessive)]
Quality:
Cross references:
OMIM: "Hyperchloremia (mean 109 mM)" [OMIM:Hyperchloremia (mean 109 mM)]
OMIM: "Hyperchloremia (mean 111 mM)" [OMIM:Hyperchloremia (mean 111 mM)]
OMIM: "Hyperchloremia (mean 114 mM)" [OMIM:Hyperchloremia (mean 114 mM)]
OMIM: "Hyperchloremia (mean >110 mM in both dominant and recessive)" [OMIM:Hyperchloremia (mean >110 mM in both dominant and recessive)]
Is a (Direct Parents):
HPO         Abnormality of chloride homeostasis
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of ion homeostasis(HPO:0003111)
             Abnormality of chloride homeostasis(HPO:0011422)
                Hyperchloremia(HPO:0011423)
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Arthrogryposis - renal dysfunction - cholestasis (Orphanet:2697)
Pseudohypoaldosteronism type 2B (Orphanet:88939)
Pseudohypoaldosteronism type 2C (Orphanet:88940)
Pseudohypoaldosteronism type 2D (Orphanet:300525)
Pseudohypoaldosteronism type 2E (Orphanet:300530)