Pyloric stenosis
Symptom Information:
Symptom ID: | HPO:0002021 | ||||||||||||||||||||||||||
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) Abnormality of the stomach(HPO:0002577) Abnormality of the pylorus(HPO:0004400) Pyloric stenosis(HPO:0002021) MedDRA: Congenital, familial and genetic disorders(MedDRA:10010331) Gastrointestinal tract disorders congenital(MedDRA:10018018) Gastric disorders congenital(MedDRA:10017780) Pyloric stenosis(HPO:0002021) Gastrointestinal disorders(MedDRA:10017947) Gastrointestinal stenosis and obstruction(MedDRA:10018008) Gastric and pyloric stenosis and obstruction(MedDRA:10017752) Pyloric stenosis(HPO:0002021) |
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Database Frequency: | 51 / 7739 | ||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
1p36 deletion syndrome | (Orphanet:1606) |
2q37 microdeletion syndrome | (Orphanet:1001) |
ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY | (OMIM:614262) |
Apert syndrome | (Orphanet:87) |
Arterial tortuosity syndrome | (Orphanet:3342) |
Branchio-oculo-facial syndrome | (Orphanet:1297) |
CORNELIA DE LANGE SYNDROME 1 | (OMIM:122470) |
Chronic granulomatous disease | (Orphanet:379) |
Chronic intestinal pseudo-obstruction | (Orphanet:2978) |
Citrullinemia type I | (Orphanet:247525) |
Congenital nephrotic syndrome, Finnish type | (Orphanet:839) |
Congenital short bowel syndrome | (Orphanet:2301) |
Cornelia de Lange syndrome | (Orphanet:199) |
Costello syndrome | (Orphanet:3071) |
Craniofacial dyssynostosis | (Orphanet:1516) |
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies | (Orphanet:221145) |
Distal 22q11.2 microdeletion syndrome | (Orphanet:261330) |
EXTERNAL AUDITORY CANAL, BILATERAL ATRESIA OF, WITH CONGENITAL VERTICALTALUS | (OMIM:133705) |
Ehlers-Danlos syndrome with periventricular heterotopia | (Orphanet:82004) |
Epidermolysis bullosa simplex | (Orphanet:304) |
Generalized congenital lipodystrophy with myopathy | (Orphanet:228429) |
Harrod syndrome | (Orphanet:2115) |
Hennekam syndrome | (Orphanet:2136) |
Hypoparathyroidism - deafness - renal disease | (Orphanet:2237) |
INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED | (OMIM:300048) |
Jacobsen syndrome | (Orphanet:2308) |
Junctional epidermolysis bullosa - pyloric atresia | (Orphanet:79403) |
Junctional epidermolysis bullosa, Herlitz type | (Orphanet:79404) |
Junctional epidermolysis bullosa, non-Herlitz type | (Orphanet:89840) |
Kleefstra syndrome | (Orphanet:261494) |
Knobloch syndrome | (Orphanet:1571) |
Koolen-De Vries syndrome | (Orphanet:96169) |
Lowry-MacLean syndrome | (Orphanet:2409) |
MICROPHTHALMIA, SYNDROMIC 1 | (OMIM:309800) |
Marden-Walker syndrome | (Orphanet:2461) |
OPITZ-KAVEGGIA SYNDROME | (OMIM:305450) |
OSTEOGENESIS IMPERFECTA, TYPE X | (OMIM:613848) |
Ornithine transcarbamylase deficiency | (Orphanet:664) |
PYLORIC STENOSIS, INFANTILE HYPERTROPHIC, 1 | (OMIM:179010) |
Paris-Trousseau thrombocytopenia | (Orphanet:851) |
Pericardial and diaphragmatic defect | (Orphanet:2847) |
Postaxial acrofacial dysostosis | (Orphanet:246) |
Proximal 16p11.2 microdeletion syndrome | (Orphanet:261197) |
Renal cysts and diabetes syndrome | (Orphanet:93111) |
Rothmund-Thomson syndrome | (Orphanet:2909) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
TRANSPOSITION OF THE GREAT ARTERIES, DEXTRO-LOOPED 2 | (OMIM:613853) |
Ulnar-mammary syndrome | (Orphanet:3138) |
X-linked centronuclear myopathy | (Orphanet:596) |
Yunis-Varon syndrome | (Orphanet:3472) |
Zellweger syndrome | (Orphanet:912) |