Reduced consciousness/confusion

Symptom Information:

Symptom ID: HPO:0004372
Synonyms:
Disturbances of consciousness [HPO:0004372]
Lowered consciousness [HPO:0004372]
Disturbances of consciousness [OMIM:Disturbances of consciousness]
Disturbance of consciousness [OMIM:Disturbance of consciousness]
Quality:
Cross references:
OMIM: "Disturbances of consciousness" [OMIM:Disturbances of consciousness]
OMIM: "Disturbance of consciousness" [OMIM:Disturbance of consciousness]
Is a (Direct Parents):
HPO         Abnormality of higher mental function
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)
MedDRA:
Database Frequency: 73 / 7739
Resource:

All diseases associated with this symptom:

Acute intermittent porphyria (Orphanet:79276)
Autosomal dominant hypocalcemia (Orphanet:428)
Autosomal dominant hypophosphatemic rickets (Orphanet:89937)
Babesiosis (Orphanet:108)
Behçet disease (Orphanet:117)
Benign familial infantile seizures (Orphanet:306)
Biotinidase deficiency (Orphanet:79241)
CADASIL (Orphanet:136)
Canavan disease (Orphanet:141)
Carnitine palmitoyl transferase 1A deficiency (Orphanet:156)
Carnitine palmitoyl transferase II deficiency (Orphanet:157)
Central diabetes insipidus (Orphanet:178029)
Cholera (Orphanet:173)
Cholesteryl ester storage disease (Orphanet:75234)
Citrullinemia type II (Orphanet:247585)
Classic galactosemia (Orphanet:79239)
Cogan syndrome (Orphanet:1467)
Congenital thrombotic thrombocytopenic purpura due to ADAMTS-13 deficiency (Orphanet:93583)
Crigler-Najjar syndrome (Orphanet:205)
Cushing disease (Orphanet:96253)
Cushing syndrome (Orphanet:553)
Dengue fever (Orphanet:99828)
Ebola hemorrhagic fever (Orphanet:319218)
Ehlers-Danlos syndrome, classic type (Orphanet:287)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Febrile infection-related epilepsy syndrome (Orphanet:163703)
GTP cyclohydrolase I deficiency (Orphanet:2102)
Galactosemia (Orphanet:352)
Glutaryl-CoA dehydrogenase deficiency (Orphanet:25)
Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1 (Orphanet:137681)
Hereditary central diabetes insipidus (Orphanet:30925)
Hereditary cerebral hemorrhage with amyloidosis, Italian type (Orphanet:324713)
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type (Orphanet:324703)
Hereditary coproporphyria (Orphanet:79273)
Holocarboxylase synthetase deficiency (Orphanet:79242)
Homocystinuria without methylmalonic aciduria (Orphanet:622)
Lassa fever (Orphanet:99824)
Legionellosis (Orphanet:549)
Lujo hemorrhagic fever (Orphanet:319213)
MELAS (Orphanet:550)
Marburg hemorrhagic fever (Orphanet:99826)
Metachromatic leukodystrophy (Orphanet:512)
Methylmalonic acidemia with homocystinuria (Orphanet:26)
Methylmalonic acidemia with homocystinuria, type cblC (Orphanet:79282)
Methylmalonic acidemia with homocystinuria, type cblD (Orphanet:79283)
Methylmalonic acidemia with homocystinuria, type cblF (Orphanet:79284)
Methylmalonic acidemia without homocystinuria (Orphanet:293355)
Multiple carboxylase deficiency (Orphanet:148)
Multiple endocrine neoplasia type 2 (Orphanet:653)
Neuroferritinopathy (Orphanet:157846)
Nipah virus disease (Orphanet:99825)
Pellagra-like skin rash-neurological manifestations (Orphanet:2837)
Porphyria cutanea tarda (Orphanet:101330)
Pyruvate dehydrogenase deficiency (Orphanet:765)
Pyruvate dehydrogenase lipoic acid synthetase deficiency (OMIM:614462)
Pyruvate dehydrogenase phosphatase deficiency (Orphanet:79246)
Rabies (Orphanet:770)
Rift valley fever (Orphanet:319251)
Scrub typhus (Orphanet:83317)
Secondary polycythemia (Orphanet:98428)
Severe Canavan disease (Orphanet:314911)
Spontaneous periodic hypothermia (Orphanet:29822)
Takayasu arteritis (Orphanet:3287)
Thrombotic thrombocytopenic purpura (Orphanet:54057)
Typhoid (Orphanet:99745)
Viral hemorrhagic fever (Orphanet:341)
Vitamin B12-responsive methylmalonic acidemia (Orphanet:28)
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)
Waldenström macroglobulinemia (Orphanet:33226)
Wyburn-Mason syndrome (Orphanet:53719)
Yellow fever (Orphanet:99829)