Meckel diverticulum
Symptom Information:
Symptom ID: | HPO:0002245 | ||||||||||
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) 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) |
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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) |