Abnormality of the stomach

Symptom Information:

Symptom ID: HPO:0002577
Synonyms:
Stomach anomaly [Orphanet:26260]
Congenital anomaly of stomach (disorder) [Orphanet:26260]
Stomach/gastric anomaly [Orphanet:26260]
Congenital gastric anomaly [Orphanet:26260]
Congenital gastric anomaly [MedDRA:10061063]
Congenital gastric anomaly NOS [MedDRA:10061063]
Other specified congenital anomalies of stomach [MedDRA:10061063]
Quality:
Cross references:
Orphanet:26260 "Stomach/gastric anomaly" [Orphanet:26260]
Is a (Direct Parents):
Orphanet Structural anomalies of the digestive tract
MedDRA Gastric disorders congenital
HPO         Abnormality of the gastrointestinal tract
HPO         Gastric varix
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 stomach(HPO:0002577)
MedDRA:
Congenital, familial and genetic disorders(MedDRA:10010331)
    Gastrointestinal tract disorders congenital(MedDRA:10018018)
       Gastric disorders congenital(MedDRA:10017780)
          Abnormality of the stomach(HPO:0002577)
Database Frequency: 84 / 7739
Resource:

All diseases associated with this symptom:

14q12 microdeletion syndrome (Orphanet:261144)
16p11.2p12.2 microdeletion syndrome (Orphanet:261211)
16p13.11 microdeletion syndrome (Orphanet:261236)
17p11.2 microduplication syndrome (Orphanet:1713)
17q23.1q23.2 microdeletion syndrome (Orphanet:261279)
1p36 deletion syndrome (Orphanet:1606)
1q21.1 microduplication syndrome (Orphanet:250994)
22q11.2 deletion syndrome (Orphanet:567)
3C syndrome (Orphanet:7)
3q29 microdeletion syndrome (Orphanet:65286)
48,XXXY syndrome (Orphanet:96263)
49,XXXXY syndrome (Orphanet:96264)
8q12 microduplication syndrome (Orphanet:228399)
Acro-pectoro-renal dysplasia (Orphanet:956)
Aicardi syndrome (Orphanet:50)
Alpha-N-acetylgalactosaminidase deficiency (Orphanet:3137)
Alpha-thalassemia - X-linked intellectual deficit syndrome (Orphanet:847)
Apert syndrome (Orphanet:87)
Arterial tortuosity syndrome (Orphanet:3342)
Axial mesodermal dysplasia spectrum (Orphanet:1834)
Bohring-Opitz syndrome (Orphanet:97297)
CHARGE syndrome (Orphanet:138)
Canavan disease (Orphanet:141)
Christianson syndrome (Orphanet:85278)
Chronic hiccup (Orphanet:396)
Congenital pulmonary lymphangiectasia (Orphanet:2414)
Corneal anesthesia - deafness - intellectual deficit (Orphanet:1051)
Cornelia de Lange syndrome (Orphanet:199)
Costello syndrome (Orphanet:3071)
Diffuse cutaneous systemic sclerosis (Orphanet:220393)
Ehlers-Danlos syndrome type 1 (Orphanet:90309)
Ehlers-Danlos syndrome type 2 (Orphanet:90318)
Ehlers-Danlos syndrome type 7B (Orphanet:99876)
Ehlers-Danlos syndrome with periventricular heterotopia (Orphanet:82004)
Ehlers-Danlos syndrome, classic type (Orphanet:287)
Ehlers-Danlos syndrome, dermatosparaxis type (Orphanet:1901)
Ehlers-Danlos syndrome, hypermobility type (Orphanet:285)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
Epidermolysis bullosa simplex with pyloric atresia (Orphanet:158684)
Esophageal adenocarcinoma (Orphanet:99976)
Esophageal carcinoma (Orphanet:70482)
Fabry disease (Orphanet:324)
Familial dysautonomia (Orphanet:1764)
Focal dermal hypoplasia (Orphanet:2092)
Fragile X syndrome (Orphanet:908)
Fryns syndrome (Orphanet:2059)
Gastrocutaneous syndrome (Orphanet:2069)
Genitopatellar syndrome (Orphanet:85201)
Haddad syndrome (Orphanet:99803)
Hereditary folate malabsorption (Orphanet:90045)
Hereditary hyperekplexia (Orphanet:3197)
Holoprosencephaly (Orphanet:2162)
Intellectual deficit - hypoplastic corpus callosum - preauricular tag (Orphanet:1495)
Isolated polycystic liver disease (Orphanet:2924)
Junctional epidermolysis bullosa (Orphanet:305)
Junctional epidermolysis bullosa - pyloric atresia (Orphanet:79403)
Juvenile polyposis syndrome (Orphanet:2929)
Kleefstra syndrome (Orphanet:261494)
Lacrimo-auriculo-dento-digital syndrome (Orphanet:2363)
Limited cutaneous systemic sclerosis (Orphanet:220402)
Microgastria - limb reduction defect (Orphanet:2538)
Occipital horn syndrome (Orphanet:198)
Oculocerebrorenal syndrome (Orphanet:534)
Omphalocele syndrome, Shprintzen-Goldberg type (Orphanet:3164)
Palmoplantar keratoderma-esophageal carcinoma syndrome (Orphanet:2198)
Pantothenate kinase-associated neurodegeneration (Orphanet:157850)
Pitt-Hopkins syndrome (Orphanet:2896)
Polymyositis (Orphanet:732)
Progeria - short stature - pigmented nevi (Orphanet:2959)
Proximal 16p11.2 microdeletion syndrome (Orphanet:261197)
Reynolds syndrome (Orphanet:779)
Schwartz-Jampel syndrome (Orphanet:800)
Scleroderma (Orphanet:801)
Severe Canavan disease (Orphanet:314911)
Shprintzen-Goldberg syndrome (Orphanet:2462)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Smith-Magenis syndrome (Orphanet:819)
Stevens-Johnson syndrome (Orphanet:36426)
Stickler syndrome (Orphanet:828)
Sudden infant death - dysgenesis of the testes (Orphanet:168593)
Syndromic X-linked ichthyosis (Orphanet:281090)
Williams syndrome (Orphanet:904)
X-linked Ehlers-Danlos syndrome (Orphanet:75497)