Clubbing of fingers
Symptom Information:
Symptom ID: | HPO:0100759 | ||||||||||||||||||||||||
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 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) |
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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) |