Duodenal stenosis
Symptom Information:
Symptom ID: | HPO:0100867 | |||||||||||||||||||||
Synonyms: |
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Cross references: |
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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 duodenum(HPO:0002246) Duodenal stenosis(HPO:0100867) MedDRA: Gastrointestinal disorders(MedDRA:10017947) Gastrointestinal stenosis and obstruction(MedDRA:10018008) Duodenal and small intestinal stenosis and obstruction(MedDRA:10013811) Duodenal stenosis(HPO:0100867) Congenital, familial and genetic disorders(MedDRA:10010331) Gastrointestinal tract disorders congenital(MedDRA:10018018) Intestinal disorders congenital(MedDRA:10022646) Duodenal stenosis(HPO:0100867) |
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Database Frequency: | 29 / 7739 | |||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Annular pancreas | (Orphanet:675) |
Colonic atresia | (Orphanet:1198) |
Congenital alveolar capillary dysplasia | (Orphanet:210122) |
Congenital contractural arachnodactyly | (Orphanet:115) |
Down syndrome | (Orphanet:870) |
Duodenal atresia | (Orphanet:1203) |
Familial visceral myopathy | (Orphanet:2604) |
Fanconi anemia | (Orphanet:84) |
Feingold syndrome | (Orphanet:1305) |
Focal dermal hypoplasia | (Orphanet:2092) |
Fryns syndrome | (Orphanet:2059) |
Hypoplastic pancreas-intestinal atresia-hypoplastic gallbalder syndrome | (Orphanet:293864) |
Jacobsen syndrome | (Orphanet:2308) |
Junctional epidermolysis bullosa | (Orphanet:305) |
Junctional epidermolysis bullosa - pyloric atresia | (Orphanet:79403) |
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2 | (OMIM:614114) |
MUNGAN SYNDROME | (OMIM:611376) |
Matthew-Wood syndrome | (Orphanet:2470) |
Microphthalmia - microtia - fetal akinesia | (Orphanet:2547) |
Mirror polydactyly - vertebral segmentation - limbs defects | (Orphanet:3004) |
Mosaic variegated aneuploidy syndrome | (Orphanet:1052) |
Multiple intestinal atresia | (Orphanet:2300) |
Short rib-polydactyly syndrome | (Orphanet:1505) |
Solitary median maxillary central incisor syndrome | (Orphanet:2286) |
Thalidomide embryopathy | (Orphanet:3312) |
Thoraco-abdominal enteric duplication | (Orphanet:1759) |
Torticollis - keloids - cryptorchidism - renal dysplasia | (Orphanet:3341) |
Tracheo-esophageal fistula - hypospadias | (Orphanet:2042) |
Umbilical cord ulceration - intestinal atresia | (Orphanet:3405) |