Hepatic encephalopathy
Symptom Information:
Symptom ID: | HPO:0002480 | ||||
Synonyms: |
|
||||
Quality: | |||||
Cross references: |
|
||||
Is a (Direct Parents): |
|
||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system morphology(HPO:0012639) Morphological abnormality of the central nervous system(HPO:0002011) Encephalopathy(HPO:0001298) Hepatic encephalopathy(HPO:0002480) MedDRA: Hepatobiliary disorders(MedDRA:10019805) Hepatic and hepatobiliary disorders(MedDRA:10019654) Hepatic failure and associated disorders(MedDRA:10019664) Hepatic encephalopathy(HPO:0002480) |
||||
Database Frequency: | 6 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Carnitine uptake deficiency | (Orphanet:158) |
Citrullinemia type II | (Orphanet:247585) |
LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1 | (OMIM:308240) |
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency | (Orphanet:5) |
PATENT DUCTUS VENOSUS | (OMIM:601466) |
Very long chain acyl-CoA dehydrogenase deficiency | (Orphanet:26793) |