Abnormality of finger
Symptom Information:
Symptom ID: | HPO:0001167 | ||||||
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 digit(HPO:0011297) Abnormality of finger(HPO:0001167) MedDRA: |
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Database Frequency: | 29 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Acrofacial dysostosis, Catania type | (Orphanet:1786) |
Acromesomelic dysplasia, Hunter-Thomson type | (Orphanet:968) |
Adams-Oliver syndrome | (Orphanet:974) |
Arthrogryposis with oculomotor limitation and electroretinal anomalies | (Orphanet:1154) |
Bazex-Dupré-Christol syndrome | (Orphanet:113) |
Brachydactyly - arterial hypertension | (Orphanet:1276) |
CATARACT 5, MULTIPLE TYPES | (OMIM:116800) |
Chondrodysplasia - disorder of sex development | (Orphanet:1422) |
Cleidorhizomelic syndrome | (Orphanet:1453) |
Distal monosomy 17q | (Orphanet:1597) |
Epilepsy telangiectasia | (Orphanet:1951) |
Epiphyseal dysplasia - hearing loss - dysmorphism | (Orphanet:1825) |
Familial digital arthropathy-brachydactyly | (Orphanet:85169) |
Fanconi anemia | (Orphanet:84) |
Heart-hand syndrome type 3 | (Orphanet:1342) |
Histidinuria - renal tubular defect | (Orphanet:2158) |
Hurler syndrome | (Orphanet:93473) |
Leri pleonosteosis | (Orphanet:2900) |
Lethal faciocardiomelic dysplasia | (Orphanet:1972) |
Linear nevus sebaceus syndrome | (Orphanet:2612) |
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 | (Orphanet:2636) |
Non-rhizomelic chondrodysplasia punctata | (Orphanet:176) |
Orofaciodigital syndrome type 1 | (Orphanet:2750) |
Orofaciodigital syndrome type 3 | (Orphanet:2752) |
Paraplegia - brachydactyly - cone-shaped epiphysis | (Orphanet:2823) |
Sclerosteosis | (Orphanet:3152) |
Skeletal dysplasia - epilepsy - short stature | (Orphanet:1858) |
Triphalangeal thumbs - brachyectrodactyly | (Orphanet:2947) |
Waardenburg syndrome type 3 | (Orphanet:896) |