Gastroschisis

Symptom Information:

Symptom ID: HPO:0001543
Synonyms:
Gastroschisis (disorder) [Orphanet:17330]
Gastroschisis [Orphanet:17330]
Gastroschisis [OMIM:Gastroschisis]
Gastroschisis [MedDRA:10018046]
Quality:
Cross references:
Orphanet:17330 "Gastroschisis" [Orphanet:17330]
OMIM: "Gastroschisis" [OMIM:Gastroschisis]
UMLS:C0265706 "Gastroschisis" [HPO:0001543]
UMLS:C0265706 "Gastroschisis" [Orphanet:17330]
Is a (Direct Parents):
HPO         Abdominal wall defect
Orphanet Abnormality of the abdominal wall
MedDRA Gastrointestinal tract disorders congenital NEC
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the abdomen(HPO:0001438)
          Abnormality of the abdominal wall(HPO:0004298)
             Abdominal wall defect(HPO:0010866)
                Gastroschisis(HPO:0001543)
MedDRA:
Congenital, familial and genetic disorders(MedDRA:10010331)
    Gastrointestinal tract disorders congenital(MedDRA:10018018)
       Gastrointestinal tract disorders congenital NEC(MedDRA:10027679)
          Gastroschisis(HPO:0001543)
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

Arthrogryposis multiplex congenita (Orphanet:1037)
Colonic atresia (Orphanet:1198)
Constriction rings syndrome (Orphanet:295000)
Gastroschisis (Orphanet:2368)
Hypoglossia - hypodactyly (Orphanet:989)
Iniencephaly (Orphanet:63259)
Limb body wall complex (Orphanet:2369)
Medeira-Dennis-Donnai syndrome (Orphanet:2476)
Nager syndrome (Orphanet:245)
Terminal transverse defects of arm (Orphanet:93937)
Tetraamelia - multiple malformations (Orphanet:3301)