Clubbing
Symptom Information:
Symptom ID: | HPO:0001217 | |||||||||||||||||||||
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 skeletal system(HPO:0000924) Abnormality of skeletal morphology(HPO:0011842) Abnormal appendicular skeleton morphology(HPO:0011844) Abnormality of limb bone morphology(HPO:0002813) Abnormality of digit(HPO:0011297) Clubbing(HPO:0001217) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Musculoskeletal and connective tissue disorders NEC(MedDRA:10028393) Soft tissue disorders NEC(MedDRA:10041288) Clubbing(HPO:0001217) |
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Database Frequency: | 39 / 7739 | |||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Acro-cardio-facial syndrome | (Orphanet:2008) |
Acute interstitial pneumonia | (Orphanet:79126) |
Atelosteogenesis type I | (Orphanet:1190) |
CYANOSIS AND HEPATIC DISEASE | (OMIM:219400) |
Chronic respiratory distress with surfactant metabolism deficiency | (Orphanet:217566) |
Congenital reticular ichthyosiform erythroderma | (Orphanet:281190) |
Cranio-osteoarthropathy | (Orphanet:1525) |
Cronkhite-Canada syndrome | (Orphanet:2930) |
Desquamative interstitial pneumonia | (Orphanet:98852) |
ENTEROPATHY, PROTEIN-LOSING | (OMIM:226300) |
Gaucher disease type 1 | (Orphanet:77259) |
Gaucher disease type 2 | (Orphanet:77260) |
Gaucher disease type 3 | (Orphanet:77261) |
Generalized juvenile polyposis/juvenile polyposis coli | (Orphanet:329971) |
HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 2 | (OMIM:614441) |
Hereditary hemorrhagic telangiectasia | (Orphanet:774) |
Hereditary sclerosing poikiloderma, Weary type | (Orphanet:221039) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 4A | (OMIM:601277) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6 | (OMIM:612281) |
INFANTILE LIVER FAILURE SYNDROME 2 | (OMIM:615486) |
Idiopathic pulmonary alveolar proteinosis | (Orphanet:747) |
Idiopathic pulmonary fibrosis | (Orphanet:2032) |
Isolated adermatoglyphia | (Orphanet:289465) |
Isolated congenital digital clubbing | (Orphanet:217059) |
JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME | (OMIM:175050) |
Juvenile polyposis syndrome | (Orphanet:2929) |
Lymphoid interstitial pneumonia | (Orphanet:79128) |
MUCUS INSPISSATION OF RESPIRATORY TRACT | (OMIM:253240) |
Necrotizing encephalomyelopathy, subacute, of Leigh, adult | (OMIM:161700) |
Neonatal acute respiratory distress with surfactant metabolism deficiency | (Orphanet:217563) |
Pitt-Hopkins syndrome | (Orphanet:2896) |
Pulmonary arteriovenous fistula | (Orphanet:2038) |
Pulmonary capillary hemangiomatosis | (Orphanet:199241) |
Pulmonary venoocclusive disease | (Orphanet:31837) |
Respiratory bronchiolitis - interstitial lung disease | (Orphanet:79127) |
SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 1 | (OMIM:265120) |
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER | (OMIM:187300) |
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2 | (OMIM:600376) |
Tropical endomyocardial fibrosis | (Orphanet:75565) |