Acholic stools

Symptom Information:

Symptom ID: HPO:0011985
Synonyms:
Acholia [HPO:0011985]
Discolored, acholic stools [HPO:0011985]
Acholic stools [OMIM:Acholic stools]
Discolored, acholic stools [OMIM:Discolored, acholic stools]
Faeces pale [MedDRA:10016102]
Acholic stools [Orphanet:27420]
Pale feces (finding) [Orphanet:27420]
Acholic stool (finding) [Orphanet:27420]
Acholia [Orphanet:27420]
Mucous stools/acholic stools [Orphanet:27420]
Quality:
Cross references:
Orphanet:27420 "Mucous stools/acholic stools" [Orphanet:27420]
OMIM: "Acholic stools" [OMIM:Acholic stools]
OMIM: "Discolored, acholic stools" [OMIM:Discolored, acholic stools]
UMLS:C0948198 "Acholia" [Orphanet:27420]
UMLS:C0232720 "Pale feces (finding)" [Orphanet:27420]
Is a (Direct Parents):
Orphanet Functional anomalies of the digestive system
HPO         Cholestasis
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the abdomen(HPO:0001438)
          Abnormality of the abdominal organs(HPO:0002012)
             Abnormality of the liver(HPO:0001392)
                Abnormality of the biliary system(HPO:0004297)
                   Cholestasis(HPO:0001396)
                      Acholic stools(HPO:0011985)
MedDRA:
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

Benign recurrent intrahepatic cholestasis (Orphanet:65682)
Biliary atresia (Orphanet:30391)
Cholestasis - lymphedema (Orphanet:1414)
Congenital bile acid synthesis defect type 1 (Orphanet:79301)
Congenital bile acid synthesis defect type 3 (Orphanet:79302)
MITCHELL-RILEY SYNDROME (OMIM:615710)