Metabolic acidosis

Symptom Information:

Symptom ID: HPO:0001942
Synonyms:
Metabolic acidosis [OMIM:Metabolic acidosis]
Metabolic acidosis (transient, resolves in infancy) [OMIM:Metabolic acidosis (transient, resolves in infancy)]
Metabolic acidosis [MedDRA:10027417]
Quality:
Cross references:
OMIM: "Metabolic acidosis" [OMIM:Metabolic acidosis]
OMIM: "Metabolic acidosis (transient, resolves in infancy)" [OMIM:Metabolic acidosis (transient, resolves in infancy)]
Is a (Direct Parents):
MedDRA Metabolic acidoses (excl diabetic acidoses)
HPO         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)
                Metabolic acidosis(HPO:0001942)
MedDRA:
Metabolism and nutrition disorders(MedDRA:10027433)
    Acid-base disorders(MedDRA:10000485)
       Metabolic acidoses (excl diabetic acidoses)(MedDRA:10027416)
          Metabolic acidosis(HPO:0001942)
Database Frequency: 81 / 7739
Resource:

All diseases associated with this symptom:

3-hydroxy-3-methylglutaric aciduria (Orphanet:20)
3-methylglutaconic aciduria type 1 (Orphanet:67046)
ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2 (OMIM:613404)
Arterial calcification, generalized, of infancy, 1 (OMIM:208000)
Arthrogryposis - renal dysfunction - cholestasis (Orphanet:2697)
CARBONIC ANHYDRASE VA DEFICIENCY, HYPERAMMONEMIA DUE TO (OMIM:615751)
Cardiomyopathy-hypotonia-lactic acidosis syndrome (Orphanet:91130)
Classic galactosemia (Orphanet:79239)
Combined oxidative phosphorylation defect type 17 (Orphanet:369913)
Combined oxidative phosphorylation defect type 4 (Orphanet:254925)
Combined oxidative phosphorylation defect type 8 (Orphanet:319504)
Congenital lactase deficiency (Orphanet:53690)
Congenital lactic acidosis, Saguenay-Lac-St. Jean type (Orphanet:70472)
D-glyceric aciduria (Orphanet:941)
Dent disease type 1 (Orphanet:93622)
Dihydropyrimidinuria (Orphanet:38874)
Distal renal tubular acidosis with anemia (Orphanet:93610)
Encephalopathy due to hydroxykynureninuria (Orphanet:79155)
FANCONI RENOTUBULAR SYNDROME 3 (OMIM:615605)
Familial hyperaldosteronism type 3 (Orphanet:251274)
Fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency (Orphanet:289527)
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 (Orphanet:168566)
Fetal Gaucher disease (Orphanet:85212)
Fructose-1,6-bisphosphatase deficiency (Orphanet:348)
Fumaric aciduria (Orphanet:24)
GLYCOGEN STORAGE DISEASE Ic (OMIM:232240)
Generalized pseudohypoaldosteronism type 1 (Orphanet:171876)
Glucose-galactose malabsorption (Orphanet:35710)
Glutaryl-CoA dehydrogenase deficiency (Orphanet:25)
Hawkinsinuria (Orphanet:2118)
Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1 (Orphanet:137681)
Hereditary fructose intolerance (Orphanet:469)
Holocarboxylase synthetase deficiency (Orphanet:79242)
Hyperammonemia due to N-acetylglutamate synthetase deficiency (Orphanet:927)
Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency (Orphanet:401948)
Hypermethioninemia encephalopathy due to adenosine kinase deficiency (Orphanet:289290)
Hypotonia with lactic acidemia and hyperammonemia (Orphanet:137908)
Hypotonia-cerebral atrophy-hyperglycinemia syndrome (Orphanet:363424)
Hypouricemia, renal, 2 (OMIM:612076)
Isolated CoQ-cytochrome C reductase deficiency (Orphanet:1460)
Isolated glycerol kinase deficiency (Orphanet:408)
Isovaleric acidemia (Orphanet:33)
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (Orphanet:5)
MEDIUM CHAIN 3-KETOACYL-CoA THIOLASE DEFICIENCY (OMIM:602199)
METHYLMALONATE SEMIALDEHYDE DEHYDROGENASE DEFICIENCY (OMIM:614105)
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 3 (OMIM:615158)
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 5 (OMIM:615160)
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7 (OMIM:615824)
Malonic aciduria (Orphanet:943)
Medium chain acyl-CoA dehydrogenase deficiency (Orphanet:42)
Methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency (Orphanet:308425)
Methylmalonic acidemia with homocystinuria, type cblC (Orphanet:79282)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency (Orphanet:314637)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
Neonatal hemochromatosis (Orphanet:446)
Oxoglutaricaciduria (Orphanet:31)
Pearson syndrome (Orphanet:699)
Primary Fanconi syndrome (Orphanet:3337)
Primary hyperoxaluria (Orphanet:416)
Primary hyperoxaluria type 1 (Orphanet:93598)
Propionic acidemia (Orphanet:35)
Pseudohypoaldosteronism type 2C (Orphanet:88940)
Pseudohypoaldosteronism type 2E (Orphanet:300530)
Pyridoxal phosphate-responsive seizures (Orphanet:79096)
Pyruvate carboxylase deficiency (Orphanet:3008)
Pyruvate dehydrogenase E1-alpha deficiency (Orphanet:79243)
Pyruvate dehydrogenase E1-beta deficiency (Orphanet:255138)
Pyruvate dehydrogenase E3 deficiency (Orphanet:2394)
Pyruvate dehydrogenase E3-binding protein deficiency (Orphanet:255182)
Pyruvate dehydrogenase lipoic acid synthetase deficiency (OMIM:614462)
Pyruvate dehydrogenase phosphatase deficiency (Orphanet:79246)
RIBOFLAVIN DEFICIENCY (OMIM:615026)
Renal pseudohypoaldosteronism type 1 (Orphanet:171871)
Renal tubulopathy - encephalopathy - liver failure (Orphanet:254902)
Short chain 3-hydroxyacyl-CoA dehydrogenase deficiency (Orphanet:35123)
Short chain acyl-CoA dehydrogenase deficiency (Orphanet:26792)
Vitamin B12-responsive methylmalonic acidemia (Orphanet:28)
Vitamin B12-responsive methylmalonic acidemia type cblA (Orphanet:79310)
Vitamin B12-responsive methylmalonic acidemia type cblB (Orphanet:79311)
[DEL] ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1 (OMIM:208085)