Ulnar deviation of finger

Symptom Information:

Symptom ID: HPO:0009465
Synonyms:
Medially deviated fingers [HPO:0009465]
Ulnar deviation of the fingers [HPO:0009465]
Ulnar deviation of the fingers (finding) [Orphanet:20660]
Ulnar deviation of finger (finding) [Orphanet:20660]
Ulnar deviation of the fingers [Orphanet:20660]
Ulnar deviation of fingers [Orphanet:20660]
Ulnar deviation of fingers [OMIM:Ulnar deviation of fingers]
Ulnar deviation of fingers (neonate, resolved by early childhood) [OMIM:Ulnar deviation of fingers (neonate, resolved by early childhood)]
Ulnar deviation of the fingers [OMIM:Ulnar deviation of the fingers]
Quality:
Cross references:
HPO:0004097 "Deviation of finger" [Orphanet:20660]
Orphanet:20660 "Ulnar deviation of fingers" [Orphanet:20660]
OMIM: "Ulnar deviation of fingers" [OMIM:Ulnar deviation of fingers]
OMIM: "Ulnar deviation of fingers (neonate, resolved by early childhood)" [OMIM:Ulnar deviation of fingers (neonate, resolved by early childhood)]
OMIM: "Ulnar deviation of the fingers" [OMIM:Ulnar deviation of the fingers]
UMLS:C0231679 "Ulnar deviation of the fingers" [Orphanet:20660]
Is a (Direct Parents):
Orphanet Abnormality of the hand
HPO         Ulnar deviation of the hand or of fingers of the hand
HPO         Deviation of finger
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)
                            Deviation of finger(HPO:0004097)
                               Ulnar deviation of finger(HPO:0009465)
                         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 digit(HPO:0011297)
                      Abnormality of finger(HPO:0001167)
                         Deviation of finger(HPO:0004097)
                            Ulnar deviation of finger(HPO:0009465)
MedDRA:
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)