Coma
Symptom Information:
Symptom ID: | HPO:0001259 | |||||||||||||||
Synonyms: |
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Cross references: |
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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 the nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Abnormality of higher mental function(HPO:0011446) Reduced consciousness/confusion(HPO:0004372) Coma(HPO:0001259) MedDRA: Nervous system disorders(MedDRA:10029205) Neurological disorders NEC(MedDRA:10029305) Coma states(MedDRA:10052770) Coma(HPO:0001259) |
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Database Frequency: | 65 / 7739 | |||||||||||||||
Resource: |
All diseases associated with this symptom:
3-@METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY | (OMIM:210200) |
3-hydroxy-3-methylglutaric aciduria | (Orphanet:20) |
Acute necrotizing encephalopathy of childhood | (Orphanet:263524) |
Adenylosuccinate lyase deficiency | (Orphanet:46) |
Argininemia | (Orphanet:90) |
Argininosuccinic aciduria | (Orphanet:23) |
Atypical hemolytic uremic syndrome | (Orphanet:2134) |
Atypical hemolytic uremic syndrome with H factor anomaly | (Orphanet:93579) |
Atypical hemolytic uremic syndrome with anti-factor H antibodies | (Orphanet:93581) |
Biotin-responsive basal ganglia disease | (Orphanet:65284) |
CADASIL | (Orphanet:136) |
Carbamoylphosphate synthetase deficiency | (Orphanet:147) |
Carnitine palmitoyl transferase 1A deficiency | (Orphanet:156) |
Carnitine uptake deficiency | (Orphanet:158) |
Carnitine-acylcarnitine translocase deficiency | (Orphanet:159) |
Citrullinemia type I | (Orphanet:247525) |
Citrullinemia type II | (Orphanet:247585) |
Classic maple syrup urine disease | (Orphanet:268145) |
Cushing disease | (Orphanet:96253) |
Cushing syndrome | (Orphanet:553) |
Encephalopathy due to hydroxykynureninuria | (Orphanet:79155) |
Familial acute necrotizing encephalopathy | (Orphanet:88619) |
Familial atrial myxoma | (Orphanet:615) |
Familial glucocorticoid deficiency | (Orphanet:361) |
Familial hemophagocytic lymphohistiocytosis | (Orphanet:540) |
Familial or sporadic hemiplegic migraine | (Orphanet:569) |
Fructose-1,6-bisphosphatase deficiency | (Orphanet:348) |
GLUCOCORTICOID DEFICIENCY 1 | (OMIM:202200) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type a | (Orphanet:79258) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type b | (Orphanet:79259) |
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1 | (OMIM:267700) |
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2 | (OMIM:603553) |
HYPERLYSINURIA WITH HYPERAMMONEMIA | (OMIM:238750) |
HYPOGLYCEMIA, LEUCINE-INDUCED | (OMIM:240800) |
Hereditary fructose intolerance | (Orphanet:469) |
Holocarboxylase synthetase deficiency | (Orphanet:79242) |
Hyperammonemia due to N-acetylglutamate synthetase deficiency | (Orphanet:927) |
Hyperornithinemia-hyperammonemia-homocitrullinuria | (Orphanet:415) |
Intermittent maple syrup urine disease | (Orphanet:268173) |
Isolated 3-methylcrotonyl-CoA carboxylase deficiency | (Orphanet:6) |
Isolated NADH-CoQ reductase deficiency | (Orphanet:2609) |
Isolated glycerol kinase deficiency | (Orphanet:408) |
Isovaleric acidemia | (Orphanet:33) |
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency | (Orphanet:5) |
MELAS | (Orphanet:550) |
MIGRAINE, FAMILIAL HEMIPLEGIC, 1 | (OMIM:141500) |
MIGRAINE, FAMILIAL HEMIPLEGIC, 2 | (OMIM:602481) |
Medium chain acyl-CoA dehydrogenase deficiency | (Orphanet:42) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
Necrotizing encephalomyelopathy, subacute, of Leigh, adult | (OMIM:161700) |
Ornithine transcarbamylase deficiency | (Orphanet:664) |
Propionic acidemia | (Orphanet:35) |
Thiamine-responsive encephalopathy | (Orphanet:199348) |
Thiamine-responsive maple syrup urine disease | (Orphanet:268184) |
Typical hemolytic uremic syndrome | (Orphanet:90038) |
VISCERAL STEATOSIS, CONGENITAL | (OMIM:228100) |
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) |
Vitamin B12-unresponsive methylmalonic acidemia | (Orphanet:27) |
Vitamin B12-unresponsive methylmalonic acidemia type mut- | (Orphanet:79312) |
Vitamin B12-unresponsive methylmalonic acidemia type mut0 | (Orphanet:289916) |
WERNICKE-KORSAKOFF SYNDROME | (OMIM:277730) |
Wilson disease | (Orphanet:905) |
[DEL] GLYCOGEN STORAGE DISEASE Ib | (OMIM:232220) |