Pyloric stenosis

Symptom Information:

Symptom ID: HPO:0002021
Synonyms:
Stenosis of stomach (disorder) [Orphanet:26320]
Pyloric stenosis (disorder) [Orphanet:26320]
Pyloric Stenosis [Orphanet:26320]
Stenosis of stomach [Orphanet:26320]
Pyloric stenosis [OMIM:Pyloric stenosis]
Gastric/pyloric stenosis [Orphanet:26320]
Gastric stenosis [Orphanet:26320]
Pyloric stenosis [Orphanet:26320]
Pyloric stenosis [MedDRA:10037621]
Congenital hypertrophic pyloric stenosis [MedDRA:10037621]
Congenital pyloric stenosis [MedDRA:10037621]
Obstruction pyloric [MedDRA:10037621]
Pyloric stenosis congenital [MedDRA:10037621]
Pyloric stenosis NOS [MedDRA:10037621]
Pylorus hypertrophic congenital [MedDRA:10037621]
Stenosis pyloric [MedDRA:10037621]
Stenosis pyloric hypertrophic congenital [MedDRA:10037621]
Gastric stenosis [MedDRA:10061970]
Gastric stenosis NOS [MedDRA:10061970]
Hourglass stricture or stenosis of stomach [MedDRA:10061970]
Pyloric stenosis (1 patient) [OMIM:Pyloric stenosis (1 patient)]
Hourglass stricture or stenosis of stomach [MedDRA:10020418]
Congenital wallet stomach [Orphanet:26400]
Cascade stomach (disorder) [Orphanet:26400]
Cascade stomach [Orphanet:26400]
Congenital wallet stomach/pseudo hour-glass stomach [Orphanet:26400]
Quality:
Cross references:
Orphanet:26320 "Gastric/pyloric stenosis" [Orphanet:26320]
Orphanet:26400 "Congenital wallet stomach/pseudo hour-glass stomach" [Orphanet:26400]
OMIM: "Pyloric stenosis" [OMIM:Pyloric stenosis]
OMIM: "Pyloric stenosis (1 patient)" [OMIM:Pyloric stenosis (1 patient)]
UMLS:C0034194 "Pyloric Stenosis" [Orphanet:26320]
UMLS:C0585012 "Stenosis of stomach" [Orphanet:26320]
UMLS:C0267183 "Cascade stomach" [Orphanet:26400]
Is a (Direct Parents):
HPO         Abnormality of the pylorus
MedDRA Gastric disorders congenital
Orphanet Abnormality of the stomach
MedDRA Gastric and pyloric stenosis and obstruction
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)
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)