Respiratory alkalosis
Symptom Information:
Symptom ID: | HPO:0001950 | ||||
Synonyms: |
|
||||
Quality: | |||||
Cross references: |
|
||||
Is a (Direct Parents): |
|
||||
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) Alkalosis(HPO:0001948) Respiratory alkalosis(HPO:0001950) MedDRA: Metabolism and nutrition disorders(MedDRA:10027433) Acid-base disorders(MedDRA:10000485) Respiratory alkaloses(MedDRA:10038663) Respiratory alkalosis(HPO:0001950) |
||||
Database Frequency: | 7 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Argininosuccinic aciduria | (Orphanet:23) |
CARBONIC ANHYDRASE VA DEFICIENCY, HYPERAMMONEMIA DUE TO | (OMIM:615751) |
Carbamoylphosphate synthetase deficiency | (Orphanet:147) |
Citrullinemia type I | (Orphanet:247525) |
Congenital lactic acidosis, Saguenay-Lac-St. Jean type | (Orphanet:70472) |
Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency | (Orphanet:401948) |
Ornithine transcarbamylase deficiency | (Orphanet:664) |