Intestinal obstruction
Symptom Information:
Symptom ID: | HPO:0005214 | |||||||||||||||||||||||||
Synonyms: |
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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) Gastrointestinal obstruction(HPO:0004796) Intestinal obstruction(HPO:0005214) MedDRA: Gastrointestinal disorders(MedDRA:10017947) Gastrointestinal stenosis and obstruction(MedDRA:10018008) Gastrointestinal stenosis and obstruction NEC(MedDRA:10018009) Intestinal obstruction(HPO:0005214) |
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Database Frequency: | 35 / 7739 | |||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
AREDYLD syndrome | (Orphanet:1133) |
Acquired angioedema | (Orphanet:91385) |
Anisakiasis | (Orphanet:1070) |
Autosomal recessive cutis laxa type 1 | (Orphanet:90349) |
Bannayan-Riley-Ruvalcaba syndrome | (Orphanet:109) |
Budd-Chiari syndrome | (Orphanet:131) |
Carney-Stratakis syndrome | (Orphanet:97286) |
Congenital hypothyroidism | (Orphanet:442) |
Desmoid tumor | (Orphanet:873) |
Desmoplastic small round cell tumor | (Orphanet:83469) |
Diabetic embryopathy | (Orphanet:1926) |
Eosinophilic granulomatosis with polyangiitis | (Orphanet:183) |
Familial Mediterranean fever | (Orphanet:342) |
Gastrointestinal stromal tumor | (Orphanet:44890) |
Granulomatosis with polyangiitis | (Orphanet:900) |
Hereditary angioedema | (Orphanet:91378) |
Hereditary nonpolyposis colon cancer | (Orphanet:144) |
Hirschsprung disease | (Orphanet:388) |
Hyperimmunoglobulinemia D with periodic fever | (Orphanet:343) |
INFLAMMATORY BOWEL DISEASE 1 | (OMIM:266600) |
Infantile myofibromatosis | (Orphanet:2591) |
MELAS | (Orphanet:550) |
Malignant peritoneal mesothelioma | (Orphanet:168811) |
Multiple endocrine neoplasia type 2 | (Orphanet:653) |
Neurologic Waardenburg-Shah syndrome | (Orphanet:163746) |
Peutz-Jeghers syndrome | (Orphanet:2869) |
Primary intestinal lymphangiectasia | (Orphanet:90362) |
Pseudomyxoma peritonei | (Orphanet:26790) |
Sanjad-Sakati syndrome | (Orphanet:2323) |
T-B+ severe combined immunodeficiency due to JAK3 deficiency | (Orphanet:35078) |
TRAPS syndrome | (Orphanet:32960) |
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE | (OMIM:601675) |
Waardenburg syndrome | (Orphanet:3440) |
Waardenburg-Shah syndrome | (Orphanet:897) |
X-linked creatine transporter deficiency | (Orphanet:52503) |