Clubbing of toes
Symptom Information:
Symptom ID: | HPO:0100760 | ||||||||||||||||||
Synonyms: |
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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 lower limb(HPO:0002814) Abnormality of the foot(HPO:0001760) Abnormality of toe(HPO:0001780) Abnormality of the phalanges of the toes(HPO:0010161) Clubbing of toes(HPO:0100760) Abnormality of digit(HPO:0011297) Clubbing(HPO:0001217) Clubbing of toes(HPO:0100760) Abnormality of toe(HPO:0001780) Abnormality of the phalanges of the toes(HPO:0010161) Clubbing of toes(HPO:0100760) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Musculoskeletal and connective tissue disorders NEC(MedDRA:10028393) Soft tissue disorders NEC(MedDRA:10041288) Clubbing of toes(HPO:0100760) |
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Database Frequency: | 24 / 7739 | ||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Acroosteolysis, dominant type | (Orphanet:955) |
Acute interstitial pneumonia | (Orphanet:79126) |
Campomelia, Cumming type | (Orphanet:1318) |
Cranio-osteoarthropathy | (Orphanet:1525) |
Fanconi anemia | (Orphanet:84) |
Fountain syndrome | (Orphanet:3219) |
Hidrotic ectodermal dysplasia | (Orphanet:189) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 4A | (OMIM:601277) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6 | (OMIM:612281) |
Idiopathic pulmonary alveolar proteinosis | (Orphanet:747) |
Idiopathic pulmonary fibrosis | (Orphanet:2032) |
Intellectual deficit - sparse hair - brachydactyly | (Orphanet:3051) |
Lymphoid interstitial pneumonia | (Orphanet:79128) |
MUCUS INSPISSATION OF RESPIRATORY TRACT | (OMIM:253240) |
Nakajo-Nishimura syndrome | (Orphanet:2615) |
Necrotizing encephalomyelopathy, subacute, of Leigh, adult | (OMIM:161700) |
Pachydermoperiostosis | (Orphanet:2796) |
Palmoplantar keratoderma-esophageal carcinoma syndrome | (Orphanet:2198) |
Patent arterial duct | (Orphanet:706) |
Pulmonary arteriovenous fistula | (Orphanet:2038) |
Rubinstein-Taybi syndrome | (Orphanet:783) |
Secondary polycythemia | (Orphanet:98428) |
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2 | (OMIM:600376) |
Zunich-Kaye syndrome | (Orphanet:3474) |