Meckel diverticulum

Symptom Information:

Symptom ID: HPO:0002245
Synonyms:
Meckel's diverticulum (morphologic abnormality) [Orphanet:26600]
Meckel's diverticulum (disorder) [Orphanet:26600]
Meckel Diverticulum [Orphanet:26600]
Meckel diverticulum [OMIM:Meckel diverticulum]
Meckel diverticulum [Orphanet:26600]
Meckel's diverticulum [HPO:0002245]
Meckel's diverticulum [Orphanet:26600]
Vitello-intestinal duct remnant [MedDRA:10066969]
Diverticulum Meckel's [MedDRA:10066969]
Meckel's diverticulum [MedDRA:10066969]
Quality:
Cross references:
Orphanet:26600 "Meckel diverticulum" [Orphanet:26600]
OMIM: "Meckel diverticulum" [OMIM:Meckel diverticulum]
UMLS:C0025037 "Meckel Diverticulum" [Orphanet:26600]
Is a (Direct Parents):
Orphanet Abnormality of the small intestine
HPO         Abnormality of the ileum
MedDRA Intestinal disorders congenital
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)
                   Abnormality of the small intestine(HPO:0002244)
                      Abnormality of the ileum(HPO:0001549)
                         Meckel diverticulum(HPO:0002245)
MedDRA:
Congenital, familial and genetic disorders(MedDRA:10010331)
    Gastrointestinal tract disorders congenital(MedDRA:10018018)
       Intestinal disorders congenital(MedDRA:10022646)
          Meckel diverticulum(HPO:0002245)
Database Frequency: 12 / 7739
Resource:

All diseases associated with this symptom:

Congenital alveolar capillary dysplasia (Orphanet:210122)
Fanconi anemia (Orphanet:84)
Fryns syndrome (Orphanet:2059)
Hurler syndrome (Orphanet:93473)
Intellectual deficit, X-linked, Kroes type (Orphanet:163961)
Isolated trigonocephaly (Orphanet:3366)
MECKEL DIVERTICULUM (OMIM:155140)
Pericardial and diaphragmatic defect (Orphanet:2847)
SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION,LETHAL (OMIM:602613)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
TRIGONOCEPHALY 1 (OMIM:190440)
Thrombocytopenia - absent radius (Orphanet:3320)