Abnormality of the stomach
Symptom Information:
Symptom ID: | HPO:0002577 | ||||||||
Synonyms: |
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Quality: | |||||||||
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) 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) |
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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) |