Duodenal atresia
Symptom Information:
Symptom ID: | HPO:0002247 | ||||||||||||
Synonyms: |
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Cross references: |
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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) Gastrointestinal atresia(HPO:0002589) Intestinal atresia(HPO:0011100) Duodenal atresia(HPO:0002247) Abnormality of the intestine(HPO:0002242) Abnormality of the small intestine(HPO:0002244) Abnormality of the duodenum(HPO:0002246) Duodenal atresia(HPO:0002247) 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) |
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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) |