Clubbing

Symptom Information:

Symptom ID: HPO:0001217
Synonyms:
Clubbing of fingers and toes [HPO:0001217]
Digital clubbing [HPO:0001217]
Toe clubbing [Orphanet:22420]
Clubbing of toes (disorder) [Orphanet:22420]
Clubbing of toes [Orphanet:22420]
Clubbing [OMIM:Clubbing]
Clubbing of fingers and toes [OMIM:Clubbing of fingers and toes]
Digital clubbing [OMIM:Digital clubbing]
Terminal broadening/clubbing of toes [Orphanet:22420]
Club toe [Orphanet:22420]
Clubbing [MedDRA:10009691]
Clubbed [MedDRA:10009691]
Clubbing of fingers [MedDRA:10009691]
Clubbing of nails [MedDRA:10009691]
Finger clubbing [MedDRA:10009691]
Finger top hypertrophy [MedDRA:10009691]
Club toe [MedDRA:10009691]
Clubbing (rare) [OMIM:Clubbing (rare)]
Clubbing of nails (in some patients) [OMIM:Clubbing of nails (in some patients)]
Finger clubbing (seen in up to 50% of patients) [OMIM:Finger clubbing (seen in up to 50% of patients)]
Toe clubbing [OMIM:Toe clubbing]
Quality:
Cross references:
HPO:0100760 "Clubbing of toes" [Orphanet:22420]
Orphanet:22420 "Terminal broadening/clubbing of toes" [Orphanet:22420]
OMIM: "Clubbing" [OMIM:Clubbing]
OMIM: "Clubbing of fingers and toes" [OMIM:Clubbing of fingers and toes]
OMIM: "Digital clubbing" [OMIM:Digital clubbing]
OMIM: "Clubbing (rare)" [OMIM:Clubbing (rare)]
OMIM: "Clubbing of nails (in some patients)" [OMIM:Clubbing of nails (in some patients)]
OMIM: "Finger clubbing (seen in up to 50% of patients)" [OMIM:Finger clubbing (seen in up to 50% of patients)]
OMIM: "Toe clubbing" [OMIM:Toe clubbing]
UMLS:C0149651 "Clubbing" [HPO:0001217]
UMLS:C0241414 "Clubbing of toes" [Orphanet:22420]
Is a (Direct Parents):
MedDRA Soft tissue disorders NEC
Orphanet Abnormality of the foot
HPO         Abnormality of digit
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)
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)