Ulnar deviation of finger
Symptom Information:
Symptom ID: | HPO:0009465 | |||||||||
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 upper limb(HPO:0002817) Abnormality of the hand(HPO:0001155) Deviation of the hand or of fingers of the hand(HPO:0009484) Ulnar deviation of the hand or of fingers of the hand(HPO:0001193) Ulnar deviation of finger(HPO:0009465) Deviation of finger(HPO:0004097) Ulnar deviation of finger(HPO:0009465) Abnormality of finger(HPO:0001167) Deviation of finger(HPO:0004097) Ulnar deviation of finger(HPO:0009465) Abnormality of digit(HPO:0011297) Abnormality of finger(HPO:0001167) Deviation of finger(HPO:0004097) Ulnar deviation of finger(HPO:0009465) MedDRA: |
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Database Frequency: | 48 / 7739 | |||||||||
Resource: |
All diseases associated with this symptom:
Abruzzo-Erickson syndrome | (Orphanet:921) |
Acrocraniofacial dysostosis | (Orphanet:949) |
Anophthalmia - megalocornea - cardiopathy - skeletal anomalies | (Orphanet:1101) |
Arthrogryposis multiplex congenita | (Orphanet:1037) |
Bangstad syndrome | (Orphanet:1227) |
Bohring-Opitz syndrome | (Orphanet:97297) |
Brachydactyly type C | (Orphanet:93384) |
C syndrome | (Orphanet:1308) |
COLD-INDUCED SWEATING SYNDROME 1 | (OMIM:272430) |
Camptobrachydactyly | (Orphanet:1319) |
Carey-Fineman-Ziter syndrome | (Orphanet:1358) |
Cataract - intellectual deficit - hypogonadism | (Orphanet:1387) |
Cleft palate - large ears - small head | (Orphanet:2013) |
Congenital contractural arachnodactyly | (Orphanet:115) |
Costello syndrome | (Orphanet:3071) |
Craniofacial-deafness-hand syndrome | (Orphanet:1529) |
DIGITOTALAR DYSMORPHISM | (OMIM:126050) |
Diastrophic dwarfism | (Orphanet:628) |
Digitotalar dysmorphism | (Orphanet:1146) |
Distal 22q11.2 microdeletion syndrome | (Orphanet:261330) |
EPIPHYSEAL DYSPLASIA, BAUMANN TYPE | (OMIM:610797) |
Edinburgh malformation syndrome | (Orphanet:1895) |
Freeman-Sheldon syndrome | (Orphanet:2053) |
Frontometaphyseal dysplasia | (Orphanet:1826) |
Fuhrmann syndrome | (Orphanet:2854) |
Gordon syndrome | (Orphanet:376) |
Hypertryptophanemia | (Orphanet:2224) |
Intellectual disability-developmental delay-contractures syndrome | (Orphanet:3454) |
Langer mesomelic dysplasia | (Orphanet:2632) |
Lichstenstein syndrome | (Orphanet:2390) |
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III | (OMIM:210730) |
Malignant hyperthermia - arthrogryposis - torticollis | (Orphanet:2215) |
Mesomelia-synostoses syndrome | (Orphanet:2496) |
Mesomelic dwarfism, Reinhardt-Pfeiffer type | (Orphanet:2634) |
Mesomelic dysplasia, Kantaputra type | (Orphanet:1836) |
Neuroectodermal-endocrine syndrome | (Orphanet:2676) |
PHAVER syndrome | (Orphanet:2876) |
Polyneuropathy - intellectual deficit - acromicria - premature menopause | (Orphanet:2928) |
Say-Barber-Miller syndrome | (Orphanet:3132) |
Sheldon-Hall syndrome | (Orphanet:1147) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
Stüve-Wiedemann syndrome | (Orphanet:3206) |
Syndactyly type 5 | (Orphanet:93406) |
Syndrome with brachydactyly | (Orphanet:69028) |
Townes-Brocks syndrome | (Orphanet:857) |
Ulna hypoplasia - intellectual deficit | (Orphanet:2249) |
Upper limb mesomelic dysplasia | (Orphanet:2497) |
WHISTLING FACE SYNDROME, RECESSIVE FORM | (OMIM:277720) |