Intestinal obstruction

Symptom Information:

Symptom ID: HPO:0005214
Synonyms:
Intestinal occlusion [Orphanet:27630]
Intestinal obstruction (disorder) [Orphanet:27630]
Intestinal Obstruction [Orphanet:27630]
Intestinal obstruction [OMIM:Intestinal obstruction]
Intestinal obstruction/ileus [Orphanet:27630]
Intestinal obstruction [Orphanet:27630]
Intestinal obstruction [MedDRA:10022687]
Bowel obstruction [MedDRA:10022687]
Impaction of intestine [MedDRA:10022687]
Impaction of intestine, unspecified [MedDRA:10022687]
Intestinal obstruction NOS [MedDRA:10022687]
Intestinal obstruction without mention of hernia [MedDRA:10022687]
Intestinal or peritoneal adhesions with obstruction [MedDRA:10022687]
Obstruction bowel [MedDRA:10022687]
Obstruction intestinal [MedDRA:10022687]
Other impaction of intestine [MedDRA:10022687]
Other specified intestinal obstruction [MedDRA:10022687]
Other specified intestinal obstruction not elsewhere classified [MedDRA:10022687]
Subacute intestinal obstruction [MedDRA:10022687]
Unspecified intestinal obstruction [MedDRA:10022687]
Partial bowel obstruction [MedDRA:10022687]
Chronic intestinal obstruction [MedDRA:10022687]
Bowel obstruction [OMIM:Bowel obstruction]
Intestinal ileus [Orphanet:27630]
Ileus [Orphanet:27630]
Quality:
Cross references:
Orphanet:27630 "Intestinal obstruction/ileus" [Orphanet:27630]
OMIM: "Intestinal obstruction" [OMIM:Intestinal obstruction]
OMIM: "Bowel obstruction" [OMIM:Bowel obstruction]
UMLS:C0021843 "Intestinal Obstruction" [Orphanet:27630]
UMLS:C1258215 "Ileus" [Orphanet:27630]
Is a (Direct Parents):
MedDRA Gastrointestinal stenosis and obstruction NEC
HPO         Gastrointestinal obstruction
Orphanet Ileus
Orphanet Functional anomalies of the digestive system
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)
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)