Intestinal lymphangiectasia
Symptom Information:
Symptom ID: | HPO:0002593 | ||||
Synonyms: |
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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 abdomen(HPO:0001438) Abnormality of the abdominal organs(HPO:0002012) Abnormality of the gastrointestinal tract(HPO:0011024) Abnormality of the intestine(HPO:0002242) Intestinal lymphangiectasia(HPO:0002593) MedDRA: Gastrointestinal disorders(MedDRA:10017947) Malabsorption conditions(MedDRA:10025477) Malabsorption(HPO:0002024) Intestinal lymphangiectasia(HPO:0002593) |
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Database Frequency: | 6 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Aplasia cutis congenita - intestinal lymphangiectasia | (Orphanet:1116) |
HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2 | (OMIM:616006) |
Hennekam syndrome | (Orphanet:2136) |
Intestinal lymphangiectasia | (Orphanet:36204) |
Noonan syndrome | (Orphanet:648) |
Primary intestinal lymphangiectasia | (Orphanet:90362) |