Duodenal atresia

Symptom Information:

Symptom ID: HPO:0002247
Synonyms:
Congenital atresia of duodenum [HPO:0002247]
Congenital atresia of duodenum (disorder) [Orphanet:26480]
Duodenal atresia [Orphanet:26480]
Duodenal atresia [OMIM:Duodenal atresia]
Duodenal atresia/stenosis/megaduodenum [Orphanet:26480]
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:0100867 "Duodenal stenosis" [Orphanet:26480]
Orphanet:26480 "Duodenal atresia/stenosis/megaduodenum" [Orphanet:26480]
OMIM: "Duodenal atresia" [OMIM:Duodenal atresia]
OMIM: "Duodenal atresia (in 1/4 patients)" [OMIM:Duodenal atresia (in 1/4 patients)]
OMIM: "Megaduodenum" [OMIM:Megaduodenum]
UMLS:C0266174 "Duodenal atresia" [Orphanet:26480]
UMLS:C0266177 "Megaduodenum" [Orphanet:26480]
Is a (Direct Parents):
MedDRA Intestinal disorders congenital
Orphanet Abnormality of the small intestine
HPO         Abnormality of the duodenum
HPO         Intestinal 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)
                   Intestinal atresia(HPO:0011100)
                      Duodenal atresia(HPO:0002247)
                   Abnormality of the small intestine(HPO:0002244)
                      Abnormality of the duodenum(HPO:0002246)
                         Duodenal atresia(HPO:0002247)
                Gastrointestinal atresia(HPO:0002589)
                   Intestinal atresia(HPO:0011100)
                      Duodenal atresia(HPO:0002247)
MedDRA:
Congenital, familial and genetic disorders(MedDRA:10010331)
    Gastrointestinal tract disorders congenital(MedDRA:10018018)
       Intestinal disorders congenital(MedDRA:10022646)
          Duodenal atresia(HPO:0002247)
Database Frequency: 13 / 7739
Resource:

All diseases associated with this symptom:

CHARGE syndrome (Orphanet:138)
Congenital alveolar capillary dysplasia (Orphanet:210122)
Duodenal atresia (Orphanet:1203)
FEINGOLD SYNDROME 1 (OMIM:164280)
Familial visceral myopathy (Orphanet:2604)
Feingold syndrome (Orphanet:1305)
Fryns syndrome (Orphanet:2059)
Hypoplastic pancreas-intestinal atresia-hypoplastic gallbalder syndrome (Orphanet:293864)
MITCHELL-RILEY SYNDROME (OMIM:615710)
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2 (OMIM:614114)
MUNGAN SYNDROME (OMIM:611376)
Miller-Dieker syndrome (Orphanet:531)
Townes-Brocks syndrome (Orphanet:857)