Hiatus hernia
Symptom Information:
Symptom ID: | HPO:0002036 | ||||||||||||||||||||||||
Synonyms: |
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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) 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) |
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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) |