Interstitial pulmonary disease
Symptom Information:
Symptom ID: | HPO:0006530 | |||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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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 respiratory system(HPO:0002086) Abnormal respiratory system morphology(HPO:0012252) Abnormality of lung morphology(HPO:0002088) Interstitial pulmonary disease(HPO:0006530) MedDRA: Respiratory, thoracic and mediastinal disorders(MedDRA:10038738) Lower respiratory tract disorders (excl obstruction and infection)(MedDRA:10024967) Parenchymal lung disorders NEC(MedDRA:10033979) Interstitial pulmonary disease(HPO:0006530) |
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Database Frequency: | 26 / 7739 | |||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
AARSKOG SYNDROME, AUTOSOMAL DOMINANT | (OMIM:100050) |
Aarskog-Scott syndrome | (Orphanet:915) |
Acute interstitial pneumonia | (Orphanet:79126) |
Combined pulmonary fibrosis-emphysema syndrome | (Orphanet:300564) |
Congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome | (Orphanet:306504) |
Cryptogenic organizing pneumonia | (Orphanet:1302) |
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 1 | (OMIM:224230) |
Desquamative interstitial pneumonia | (Orphanet:98852) |
Gaucher disease type 1 | (Orphanet:77259) |
Gaucher disease type 2 | (Orphanet:77260) |
Gaucher disease type 3 | (Orphanet:77261) |
HERMANSKY-PUDLAK SYNDROME 1 | (OMIM:203300) |
Hermansky-Pudlak syndrome with pulmonary fibrosis | (Orphanet:231500) |
IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY | (OMIM:614700) |
INFANTILE LIVER FAILURE SYNDROME 2 | (OMIM:615486) |
Idiopathic pulmonary fibrosis | (Orphanet:2032) |
Immunodeficiency with natural-killer cell deficiency | (Orphanet:75391) |
Lymphangioleiomyomatosis | (Orphanet:538) |
Lymphoid interstitial pneumonia | (Orphanet:79128) |
Neonatal acute respiratory distress with surfactant metabolism deficiency | (Orphanet:217563) |
Non-specific interstitial pneumonia | (Orphanet:91364) |
Respiratory bronchiolitis - interstitial lung disease | (Orphanet:79127) |
STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET | (OMIM:615934) |
Sarcoidosis | (Orphanet:797) |
Sterile multifocal osteomyelitis with periostitis and pustulosis | (Orphanet:210115) |
Systemic sclerosis | (Orphanet:90291) |