Duodenal stenosis

Symptom Information:

Symptom ID: HPO:0100867
Synonyms:
Duodenal stenosis/atresia [HPO:0100867]
Duodenal atresia [Orphanet:26480]
Stenosis of duodenum [HPO:0100867]
Stenosis of duodenum (disorder) [Orphanet:26480]
Congenital atresia of duodenum (disorder) [Orphanet:26480]
Stenosis of duodenum [Orphanet:26480]
Duodenal stenosis [OMIM:Duodenal stenosis]
Duodenal stenosis/atresia [OMIM:Duodenal stenosis/atresia]
Duodenal atresia/stenosis/megaduodenum [Orphanet:26480]
Duodenal stenosis [Orphanet:26480]
Duodenal stenosis [MedDRA:10050094]
Duodenal stricture [MedDRA:10050094]
Duodenal stricture acquired [MedDRA:10050094]
Duodenal membranous stenosis [MedDRA:10050094]
Duodenal atresia [MedDRA:10013812]
Duodenal atresia congenital [MedDRA:10013812]
Duodenal atresia (in 1/4 patients) [OMIM:Duodenal atresia (in 1/4 patients)]
Megaduodenum [Orphanet:26480]
Megaduodenum (disorder) [Orphanet:26480]
Megaloduodenum (disorder) [Orphanet:26480]
Megaduodenum [OMIM:Megaduodenum]
Quality:
Cross references:
HPO:0002247 "Duodenal atresia" [Orphanet:26480]
Orphanet:26480 "Duodenal atresia/stenosis/megaduodenum" [Orphanet:26480]
OMIM: "Duodenal stenosis" [OMIM:Duodenal stenosis]
OMIM: "Duodenal stenosis/atresia" [OMIM:Duodenal stenosis/atresia]
OMIM: "Duodenal atresia (in 1/4 patients)" [OMIM:Duodenal atresia (in 1/4 patients)]
OMIM: "Megaduodenum" [OMIM:Megaduodenum]
UMLS:C0238093 "Stenosis of duodenum" [Orphanet:26480]
UMLS:C0266174 "Duodenal atresia" [Orphanet:26480]
UMLS:C0266177 "Megaduodenum" [Orphanet:26480]
Is a (Direct Parents):
MedDRA Duodenal and small intestinal stenosis and obstruction
HPO         Abnormality of the duodenum
MedDRA Intestinal disorders congenital
Orphanet Abnormality of the small intestine
Orphanet Duodenal atresia
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)
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)