Hepatic encephalopathy

Symptom Information:

Symptom ID: HPO:0002480
Synonyms:
Hepatic encephalopathy [OMIM:Hepatic encephalopathy]
Hepatic encephalopathy [MedDRA:10019660]
Quality:
Cross references:
OMIM: "Hepatic encephalopathy" [OMIM:Hepatic encephalopathy]
Is a (Direct Parents):
HPO         Encephalopathy
MedDRA Hepatic failure and associated disorders
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)