Hiatus hernia

Symptom Information:

Symptom ID: HPO:0002036
Synonyms:
Hiatal hernia [HPO:0002036]
Hiatal hernia (disorder) [Orphanet:27240]
Hiatal hernia [OMIM:Hiatal hernia]
Hiatus hernia [OMIM:Hiatus hernia]
Gastroesophageal reflux/pyrosis/esophagitis/hiatal hernia/gastroparesia [Orphanet:27240]
Hiatus hernia [Orphanet:27240]
Hiatus hernia [MedDRA:10020028]
Axial hiatal hernia [MedDRA:10020028]
H hernia [MedDRA:10020028]
Hernia hiatal [MedDRA:10020028]
Hiatal hernia [MedDRA:10020028]
Hiatal hernia type 1 [MedDRA:10020028]
Hiatal hernia type 2 [MedDRA:10020028]
Paraesophageal hiatal hernia [MedDRA:10020028]
Paraoesophageal hiatal hernia [MedDRA:10020028]
Rolling hiatal hernia [MedDRA:10020028]
Sliding hiatal hernia [MedDRA:10020028]
Oesophageal hernia [MedDRA:10020028]
Esophageal hernia [MedDRA:10020028]
Gastroesophageal hernia [MedDRA:10020028]
Gastrooesophageal hernia [MedDRA:10020028]
Pyrosis [MedDRA:10037676]
Heartburn (finding) [Orphanet:27240]
Heartburn [Orphanet:27240]
Quality:
Cross references:
Orphanet:27240 "Gastroesophageal reflux/pyrosis/esophagitis/hiatal hernia/gastroparesia" [Orphanet:27240]
OMIM: "Hiatal hernia" [OMIM:Hiatal hernia]
OMIM: "Hiatus hernia" [OMIM:Hiatus hernia]
UMLS:C0018834 "Heartburn" [Orphanet:27240]
Is a (Direct Parents):
Orphanet Gastroesophageal reflux
HPO         Abnormality of the stomach
Orphanet Functional anomalies of the digestive system
MedDRA Diaphragmatic disorders
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)
                   Hiatus hernia(HPO:0002036)
MedDRA:
Respiratory, thoracic and mediastinal disorders(MedDRA:10038738)
    Thoracic disorders (excl lung and pleura)(MedDRA:10013369)
       Diaphragmatic disorders(MedDRA:10012706)
          Hiatus hernia(HPO:0002036)
Database Frequency: 24 / 7739
Resource:

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
48,XXYY syndrome (Orphanet:10)
Aicardi syndrome (Orphanet:50)
Arterial tortuosity syndrome (Orphanet:3342)
Autosomal dominant Opitz G/BBB syndrome (Orphanet:306588)
Autosomal dominant spastic paraplegia type 29 (Orphanet:101009)
Autosomal dominant spastic paraplegia type 9 (Orphanet:100990)
Cornelia de Lange syndrome (Orphanet:199)
EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1 (OMIM:601776)
ESOPHAGEAL RING, LOWER (OMIM:133240)
Ehlers-Danlos syndrome due to tenascin-X deficiency (Orphanet:230839)
Ehlers-Danlos syndrome, musculocontractural type (Orphanet:2953)
Focal dermal hypoplasia (Orphanet:2092)
GASTRIC VOLVULUS, INTRATHORACIC (OMIM:137210)
Galloway-Mowat syndrome (Orphanet:2065)
Gastrocutaneous syndrome (Orphanet:2069)
HERNIA, HIATUS (OMIM:142400)
Lesch-Nyhan syndrome (Orphanet:510)
MELAS (Orphanet:550)
Noonan syndrome-like disorder with loose anagen hair (Orphanet:2701)
Occipital horn syndrome (Orphanet:198)
Opitz G/BBB syndrome (Orphanet:2745)
RIENHOFF SYNDROME (OMIM:615582)
SUCROSURIA, HIATUS HERNIA AND MENTAL RETARDATION (OMIM:272000)