Aspiration
Symptom Information:
Symptom ID: | HPO:0002835 | ||||
Synonyms: |
|
||||
Quality: | |||||
Cross references: |
|
||||
Is a (Direct Parents): |
|
||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the respiratory system(HPO:0002086) Functional respiratory abnormality(HPO:0002795) Aspiration(HPO:0002835) MedDRA: Respiratory, thoracic and mediastinal disorders(MedDRA:10038738) Respiratory disorders NEC(MedDRA:10038716) Respiratory tract disorders NEC(MedDRA:10057184) Aspiration(HPO:0002835) |
||||
Database Frequency: | 11 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant Opitz G/BBB syndrome | (Orphanet:306588) |
Distal myopathy with vocal cord weakness | (Orphanet:600) |
GM2-gangliosidosis, AB variant | (Orphanet:309246) |
Gaucher disease type 2 | (Orphanet:77260) |
Hereditary hyperekplexia | (Orphanet:3197) |
Laryngo-tracheo-esophageal cleft | (Orphanet:2004) |
Laryngo-tracheo-esophageal cleft type 3 | (Orphanet:93940) |
Opitz G/BBB syndrome | (Orphanet:2745) |
Pontine tegmental cap dysplasia | (Orphanet:269229) |
Tay-Sachs disease | (Orphanet:845) |
X-linked Opitz G/BBB syndrome | (Orphanet:306597) |