Clubbing of fingers

Symptom Information:

Symptom ID: HPO:0100759
Synonyms:
Clubbed fingers [HPO:0100759]
Clubbing (hands) [HPO:0100759]
Finger clubbing [HPO:0100759]
Finger clubbing [Orphanet:20420]
Finger clubbing (disorder) [Orphanet:20420]
Talipomanus (disorder) [Orphanet:20420]
Clubbed Fingers [Orphanet:20420]
Talipomanus [Orphanet:20420]
Clubbed fingers [OMIM:Clubbed fingers]
Clubbing of fingers [OMIM:Clubbing of fingers]
Finger clubbing [OMIM:Finger clubbing]
Terminal/third phalangeal bone of fingers broadened/deviated [Orphanet:20420]
Clubbing of fingers [Orphanet:20420]
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)]
Deviated fingertip [Orphanet:20420]
Quality:
Cross references:
Orphanet:20420 "Terminal/third phalangeal bone of fingers broadened/deviated" [Orphanet:20420]
OMIM: "Clubbed fingers" [OMIM:Clubbed fingers]
OMIM: "Clubbing of fingers" [OMIM:Clubbing of fingers]
OMIM: "Finger clubbing" [OMIM:Finger 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)]
UMLS:C0009080 "Clubbed Fingers" [Orphanet:20420]
UMLS:C0265596 "Talipomanus" [Orphanet:20420]
Is a (Direct Parents):
Orphanet Abnormality of the hand
HPO         Clubbing
Orphanet Broad fingertip
MedDRA Soft tissue disorders NEC
HPO         Abnormality of the fingertips
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 the upper limb(HPO:0002817)
                      Abnormality of the hand(HPO:0001155)
                         Abnormality of finger(HPO:0001167)
                            Abnormality of the fingertips(HPO:0001211)
                               Clubbing of fingers(HPO:0100759)
                   Abnormality of digit(HPO:0011297)
                      Abnormality of finger(HPO:0001167)
                         Abnormality of the fingertips(HPO:0001211)
                            Clubbing of fingers(HPO:0100759)
                      Clubbing(HPO:0001217)
                         Clubbing of fingers(HPO:0100759)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Musculoskeletal and connective tissue disorders NEC(MedDRA:10028393)
       Soft tissue disorders NEC(MedDRA:10041288)
          Clubbing of fingers(HPO:0100759)
Database Frequency: 40 / 7739
Resource:

All diseases associated with this symptom:

Acute interstitial pneumonia (Orphanet:79126)
Brachydactyly - elbow wrist dysplasia (Orphanet:1275)
CANDLE syndrome (Orphanet:325004)
Cartilage-hair hypoplasia (Orphanet:175)
Cataract - intellectual deficit - hypogonadism (Orphanet:1387)
Combined pulmonary fibrosis-emphysema syndrome (Orphanet:300564)
Craniosynostosis - dysmorphism - brachydactyly (Orphanet:1535)
Cronkhite-Canada syndrome (Orphanet:2930)
Epimetaphyseal skeletal dysplasia (Orphanet:1819)
Eye defects - arachnodactyly - cardiopathy (Orphanet:2725)
HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL DOMINANT (OMIM:167100)
Haim-Munk syndrome (Orphanet:2342)
Hereditary sclerosing poikiloderma, Weary type (Orphanet:221039)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 4A (OMIM:601277)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6 (OMIM:612281)
IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY (OMIM:614700)
Idiopathic pulmonary fibrosis (Orphanet:2032)
Intellectual deficit - sparse hair - brachydactyly (Orphanet:3051)
JMP syndrome (Orphanet:324999)
KETOADIPICACIDURIA (OMIM:245130)
Keipert syndrome (Orphanet:2662)
Lymphoid interstitial pneumonia (Orphanet:79128)
MUCUS INSPISSATION OF RESPIRATORY TRACT (OMIM:253240)
Metaphyseal chondrodysplasia, Jansen type (Orphanet:33067)
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 (Orphanet:2636)
Mucopolysaccharidosis type 2, attenuated form (Orphanet:217093)
NEUTROPENIA, CHRONIC FAMILIAL (OMIM:162700)
Nakajo-Nishimura syndrome (Orphanet:2615)
Naxos disease (Orphanet:34217)
Neurofaciodigitorenal syndrome (Orphanet:2673)
Non-specific interstitial pneumonia (Orphanet:91364)
Pachydermoperiostosis (Orphanet:2796)
Peutz-Jeghers syndrome (Orphanet:2869)
Proteasome disability syndrome (Orphanet:324977)
Pterygium colli - intellectual deficit - digital anomalies (Orphanet:2988)
Pulmonary arteriovenous fistula (Orphanet:2038)
Pulmonary nodular lymphoid hyperplasia (Orphanet:60026)
Rubinstein-Taybi syndrome (Orphanet:783)
Trigonocephaly - broad thumbs (Orphanet:3365)
Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome (Orphanet:65282)