Ketoacidosis
Symptom Information:
| Symptom ID: | HPO:0001993 | ||||||
| Synonyms: |
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| Is a (Direct Parents): |
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| 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) Ketoacidosis(HPO:0001993) Ketosis(HPO:0001946) Ketoacidosis(HPO:0001993) MedDRA: Metabolism and nutrition disorders(MedDRA:10027433) Acid-base disorders(MedDRA:10000485) Metabolic acidoses (excl diabetic acidoses)(MedDRA:10027416) Ketoacidosis(HPO:0001993) |
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| Database Frequency: | 17 / 7739 | ||||||
| Resource: |
All diseases associated with this symptom:
| 3-@METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY | (OMIM:210210) |
| Alström syndrome | (Orphanet:64) |
| CARBONIC ANHYDRASE VA DEFICIENCY, HYPERAMMONEMIA DUE TO | (OMIM:615751) |
| Combined malonic and methylmalonic acidemia | (Orphanet:289504) |
| DEND syndrome | (Orphanet:79134) |
| DIABETES MELLITUS, INSULIN-DEPENDENT | (OMIM:222100) |
| Diabetes mellitus, ketosis-prone | (OMIM:612227) |
| Friedreich ataxia 1 | (OMIM:229300) |
| Isolated glycerol kinase deficiency | (Orphanet:408) |
| Isovaleric acidemia | (Orphanet:33) |
| MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 | (OMIM:615453) |
| MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY | (OMIM:616095) |
| Permanent neonatal diabetes mellitus | (Orphanet:99885) |
| Pyruvate dehydrogenase E3 deficiency | (Orphanet:2394) |
| Rabson-Mendenhall syndrome | (Orphanet:769) |
| Transient neonatal diabetes mellitus | (Orphanet:99886) |
| Vitamin B12-unresponsive methylmalonic acidemia type mut0 | (Orphanet:289916) |