Coma

Symptom Information:

Symptom ID: HPO:0001259
Synonyms:
Coma (disorder) [Orphanet:43470]
Comatose [Orphanet:43470]
Coma [OMIM:Coma]
Obnubilation/coma/lethargia/desorientation [Orphanet:43470]
Coma [Orphanet:43470]
Coma [MedDRA:10010071]
Coma (non-diabetic) [MedDRA:10010071]
Coma and stupor [MedDRA:10010071]
Coma NEC [MedDRA:10010071]
Coma NOS [MedDRA:10010071]
Coma (NOS) [MedDRA:10010071]
Comatose [MedDRA:10010071]
Coma (if untreated) [OMIM:Coma (if untreated)]
Coma (in up to 33% of patients) [OMIM:Coma (in up to 33% of patients)]
Coma (less common) [OMIM:Coma (less common)]
Quality:
Cross references:
Orphanet:43470 "Obnubilation/coma/lethargia/desorientation" [Orphanet:43470]
OMIM: "Coma" [OMIM:Coma]
OMIM: "Coma (if untreated)" [OMIM:Coma (if untreated)]
OMIM: "Coma (in up to 33% of patients)" [OMIM:Coma (in up to 33% of patients)]
OMIM: "Coma (less common)" [OMIM:Coma (less common)]
UMLS:C0009421 "Coma" [HPO:0001259]
UMLS:C0009421 "Comatose" [Orphanet:43470]
Is a (Direct Parents):
MedDRA Coma states
Orphanet Lethargy
HPO         Reduced consciousness/confusion
Orphanet Sleep disturbance
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)
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)