Reduced consciousness/confusion
Symptom Information:
Symptom ID: | HPO:0004372 | ||||
Synonyms: |
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Quality: | |||||
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) MedDRA: |
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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) |