Gastroparesis

Symptom Information:

Symptom ID: HPO:0002578
Synonyms:
Gastroparesia [Orphanet:27240]
Gastroparesis [OMIM:Gastroparesis]
Gastroesophageal reflux/pyrosis/esophagitis/hiatal hernia/gastroparesia [Orphanet:27240]
Gastroparesis (less common) [OMIM:Gastroparesis (less common)]
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: "Gastroparesis" [OMIM:Gastroparesis]
OMIM: "Gastroparesis (less common)" [OMIM:Gastroparesis (less common)]
UMLS:C0152020 "Gastroparesis" [HPO:0002578]
UMLS:C0018834 "Heartburn" [Orphanet:27240]
Is a (Direct Parents):
Orphanet Gastroesophageal reflux
Orphanet Functional anomalies of the digestive system
HPO         Abnormality of the stomach
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)
                   Gastroparesis(HPO:0002578)
MedDRA:
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

48,XXYY syndrome (Orphanet:10)
Autosomal dominant progressive external ophthalmoplegia (Orphanet:254892)
Insulin-resistance syndrome type A (Orphanet:2297)
MELAS (Orphanet:550)
MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE) (OMIM:603041)
Mitochondrial neurogastrointestinal encephalomyopathy (Orphanet:298)
Oculogastrointestinal muscular dystrophy (Orphanet:1876)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 1 (OMIM:157640)
Sensory ataxic neuropathy-dysarthria-ophthalmoparesis (Orphanet:70595)
Spinocerebellar ataxia with epilepsy (Orphanet:254881)
Wolfram syndrome 1 (OMIM:222300)