Gastroesophageal reflux
Symptom Information:
Symptom ID: | HPO:0002020 | ||||||||||||||||||||||||||||||||||||
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) Gastroesophageal reflux(HPO:0002020) Abnormality of the esophagus(HPO:0002031) Gastroesophageal reflux(HPO:0002020) MedDRA: Gastrointestinal disorders(MedDRA:10017947) Gastrointestinal motility and defaecation conditions(MedDRA:10017977) Gastrointestinal atonic and hypomotility disorders NEC(MedDRA:10017933) Gastroesophageal reflux(HPO:0002020) |
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Database Frequency: | 101 / 7739 | ||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
17p11.2 microduplication syndrome | (Orphanet:1713) |
1p36 deletion syndrome | (Orphanet:1606) |
48,XXYY syndrome | (Orphanet:10) |
AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA | (OMIM:613623) |
Alpha-thalassemia - X-linked intellectual deficit syndrome | (Orphanet:847) |
Alström syndrome | (Orphanet:64) |
Aromatic L-amino acid decarboxylase deficiency | (Orphanet:35708) |
Atrioventricular defect - blepharophimosis -radial defects | (Orphanet:1352) |
Atypical Rett syndrome | (Orphanet:3095) |
Autosomal dominant spastic paraplegia type 9 | (Orphanet:100990) |
Autosomal recessive cutis laxa type 2B | (Orphanet:357064) |
Autosomal recessive spastic paraplegia type 49 | (Orphanet:320385) |
Bohring-Opitz syndrome | (Orphanet:97297) |
Branchio-oculo-facial syndrome | (Orphanet:1297) |
CARDIOFACIOCUTANEOUS SYNDROME 1 | (OMIM:115150) |
CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTALDELAY | (OMIM:616266) |
CORNELIA DE LANGE SYNDROME 1 | (OMIM:122470) |
CORNELIA DE LANGE SYNDROME 2 | (OMIM:300590) |
CORNELIA DE LANGE SYNDROME 3 | (OMIM:610759) |
CORNELIA DE LANGE SYNDROME 4 | (OMIM:614701) |
CORNELIA DE LANGE SYNDROME 5 | (OMIM:300882) |
CREST syndrome | (Orphanet:90290) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Carpenter-Waziri syndrome | (Orphanet:93973) |
Christianson syndrome | (Orphanet:85278) |
Chudley-Lowry-Hoar syndrome | (Orphanet:93971) |
Congenital nephrotic syndrome, Finnish type | (Orphanet:839) |
Cornelia de Lange syndrome | (Orphanet:199) |
Costello syndrome | (Orphanet:3071) |
Craniolenticulosutural dysplasia | (Orphanet:50814) |
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies | (Orphanet:221145) |
DDOST-CDG | (Orphanet:300536) |
Dubowitz syndrome | (Orphanet:235) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2 | (OMIM:300672) |
Ear-patella-short stature syndrome | (Orphanet:2554) |
Emanuel syndrome | (Orphanet:96170) |
Familial dysautonomia | (Orphanet:1764) |
Femoral-facial syndrome | (Orphanet:1988) |
GASTROESOPHAGEAL REFLUX | (OMIM:109350) |
Gaucher disease type 2 | (Orphanet:77260) |
Glycogen storage disease due to acid maltase deficiency, infantile onset | (Orphanet:308552) |
Hereditary sensory and autonomic neuropathy type 1B | (Orphanet:139564) |
Hereditary sensory and autonomic neuropathy type 2 | (Orphanet:970) |
Holmes-Gang syndrome | (Orphanet:93970) |
Hyperinsulinism-hyperammonemia syndrome | (Orphanet:35878) |
Hyperlysinemia, type I | (OMIM:238700) |
Hypotonia-speech impairment-severe cognitive delay syndrome | (Orphanet:371364) |
Idiopathic pulmonary fibrosis | (Orphanet:2032) |
Infantile dystonia-parkinsonism | (Orphanet:238455) |
Intellectual deficit, X-linked, Cantagrel type | (Orphanet:85277) |
Juberg-Marsidi syndrome | (Orphanet:93972) |
Kleefstra syndrome | (Orphanet:261494) |
LUBS X-LINKED MENTAL RETARDATION SYNDROME | (OMIM:300260) |
Leigh syndrome | (Orphanet:506) |
MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY | (OMIM:606369) |
MEIER-GORLIN SYNDROME 1 | (OMIM:224690) |
MEIER-GORLIN SYNDROME 2 | (OMIM:613800) |
MEIER-GORLIN SYNDROME 5 | (OMIM:613805) |
MELAS | (Orphanet:550) |
Methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency | (Orphanet:308425) |
Methylmalonic acidemia with homocystinuria, type cblJ | (Orphanet:369955) |
Microgastria - limb reduction defect | (Orphanet:2538) |
Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies | (Orphanet:369897) |
Monosomy 22q13 | (Orphanet:48652) |
Monosomy 5p | (Orphanet:281) |
Multiple congenital anomalies - hypotonia - seizures syndrome | (Orphanet:280633) |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA | (OMIM:201300) |
Navajo neurohepatopathy | (Orphanet:255229) |
Noonan syndrome | (Orphanet:648) |
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia | (Orphanet:363972) |
Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
Osteopathia striata - cranial sclerosis | (Orphanet:2780) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 4 | (OMIM:610131) |
Pediatric systemic sclerosis | (Orphanet:93567) |
Pitt-Hopkins syndrome | (Orphanet:2896) |
Pitt-Hopkins-like syndrome 2 | (OMIM:614325) |
Pontocerebellar hypoplasia type 8 | (Orphanet:324569) |
Pontocerebellar hypoplasia, type 9 | (OMIM:615809) |
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency | (Orphanet:88618) |
RETT SYNDROME, CONGENITAL VARIANT | (OMIM:613454) |
Renier-Gabreels-Jasper syndrome | (Orphanet:93975) |
Rett syndrome | (Orphanet:778) |
SLC35A2-CDG | (Orphanet:356961) |
STEVENSON-CAREY SYNDROME | (OMIM:611961) |
Severe dermatitis-multiple allergies-metabolic wasting syndrome | (Orphanet:369992) |
Severe neonatal-onset encephalopathy with microcephaly | (Orphanet:209370) |
Shprintzen-Goldberg syndrome | (Orphanet:2462) |
Smith-Fineman-Myers syndrome | (Orphanet:93974) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
Sudden infant death - dysgenesis of the testes | (Orphanet:168593) |
Systemic sclerosis | (Orphanet:90291) |
TENORIO SYNDROME | (OMIM:616260) |
Thiamine-responsive megaloblastic anemia syndrome | (Orphanet:49827) |
Timothy syndrome | (Orphanet:65283) |
Townes-Brocks syndrome | (Orphanet:857) |
WEBB-DATTANI SYNDROME | (OMIM:615926) |
Williams syndrome | (Orphanet:904) |
Wolf-Hirschhorn syndrome | (Orphanet:280) |
X-linked Opitz G/BBB syndrome | (Orphanet:306597) |
X-linked intellectual deficit - hypotonic face | (Orphanet:73220) |
X-linked spinocerebellar ataxia type 3 | (Orphanet:85297) |