Camptodactyly of finger

Symptom Information:

Symptom ID: HPO:0100490
Synonyms:
Camptodactyly (hands) [HPO:0100490]
Finger contractures [HPO:0100490]
Flexion contracture of finger [HPO:0100490]
Flexion contractures of the digits [HPO:0100490]
Flexion contractures of the fingers [HPO:0100490]
Flexion deformities of fingers [HPO:0100490]
Joint contractures of the fingers [HPO:0100490]
All fingers camptodactyly [Orphanet:20580]
Finger camptodactyly [Orphanet:20560]
Finger contractures [OMIM:Finger contractures]
Flexion contractures of the digits [OMIM:Flexion contractures of the digits]
Flexion contractures of the fingers [OMIM:Flexion contractures of the fingers]
Flexion deformities of fingers [OMIM:Flexion deformities of fingers]
Complete claw hand/camptodactyly of all fingers [Orphanet:20580]
Camptodactyly of fingers [Orphanet:20560]
Camptodactyly (2nd-5th) [OMIM:Camptodactyly (2nd-5th)]
Camptodactyly (4th and 5th fingers) [OMIM:Camptodactyly (4th and 5th fingers)]
Camptodactyly (adult) [OMIM:Camptodactyly (adult)]
Camptodactyly (present at birth) [OMIM:Camptodactyly (present at birth)]
Camptodactyly (progressive) [OMIM:Camptodactyly (progressive)]
Camptodactyly, all fingers [OMIM:Camptodactyly, all fingers]
Camptodactyly, fingers [OMIM:Camptodactyly, fingers]
Camptodactyly. [OMIM:Camptodactyly.]
Finger contractures (in some) [OMIM:Finger contractures (in some)]
Flexion contractures of fingers [OMIM:Flexion contractures of fingers]
Flexion deformity of fingers [OMIM:Flexion deformity of fingers]
Quality:
Cross references:
HPO:0005617 "Bilateral camptodactyly" [Orphanet:20580]
Orphanet:20580 "Complete claw hand/camptodactyly of all fingers" [Orphanet:20580]
Orphanet:20560 "Camptodactyly of fingers" [Orphanet:20560]
OMIM: "Finger contractures" [OMIM:Finger contractures]
OMIM: "Flexion contractures of the digits" [OMIM:Flexion contractures of the digits]
OMIM: "Flexion contractures of the fingers" [OMIM:Flexion contractures of the fingers]
OMIM: "Flexion deformities of fingers" [OMIM:Flexion deformities of fingers]
OMIM: "Camptodactyly (2nd-5th)" [OMIM:Camptodactyly (2nd-5th)]
OMIM: "Camptodactyly (4th and 5th fingers)" [OMIM:Camptodactyly (4th and 5th fingers)]
OMIM: "Camptodactyly (adult)" [OMIM:Camptodactyly (adult)]
OMIM: "Camptodactyly (present at birth)" [OMIM:Camptodactyly (present at birth)]
OMIM: "Camptodactyly (progressive)" [OMIM:Camptodactyly (progressive)]
OMIM: "Camptodactyly, all fingers" [OMIM:Camptodactyly, all fingers]
OMIM: "Camptodactyly, fingers" [OMIM:Camptodactyly, fingers]
OMIM: "Camptodactyly." [OMIM:Camptodactyly.]
OMIM: "Finger contractures (in some)" [OMIM:Finger contractures (in some)]
OMIM: "Flexion contractures of fingers" [OMIM:Flexion contractures of fingers]
OMIM: "Flexion deformity of fingers" [OMIM:Flexion deformity of fingers]
Is a (Direct Parents):
HPO         Camptodactyly
HPO         Joint contracture of the hand
Orphanet Abnormality of the hand
HPO         Abnormality of phalangeal joints of the hand
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of connective tissue(HPO:0003549)
          Flexion contracture(HPO:0001371)
             Camptodactyly(HPO:0012385)
                Camptodactyly of finger(HPO:0100490)
             Limb joint contracture(HPO:0003121)
                Contractures of the joints of the upper limbs(HPO:0100360)
                   Joint contracture of the hand(HPO:0009473)
                      Camptodactyly of finger(HPO:0100490)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle morphology(HPO:0011805)
             Flexion contracture(HPO:0001371)
                Camptodactyly(HPO:0012385)
                   Camptodactyly of finger(HPO:0100490)
                Limb joint contracture(HPO:0003121)
                   Contractures of the joints of the upper limbs(HPO:0100360)
                      Joint contracture of the hand(HPO:0009473)
                         Camptodactyly of finger(HPO:0100490)
       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 digit(HPO:0011297)
                      Abnormality of finger(HPO:0001167)
                         Abnormality of phalanx of finger(HPO:0005918)
                            Abnormality of phalangeal joints of the hand(HPO:0006261)
                               Camptodactyly of finger(HPO:0100490)
                   Abnormality of the upper limb(HPO:0002817)
                      Abnormality of upper limb joint(HPO:0009810)
                         Joint contracture of the hand(HPO:0009473)
                            Camptodactyly of finger(HPO:0100490)
                      Abnormality of the hand(HPO:0001155)
                         Abnormality of finger(HPO:0001167)
                            Abnormality of phalanx of finger(HPO:0005918)
                               Abnormality of phalangeal joints of the hand(HPO:0006261)
                                  Camptodactyly of finger(HPO:0100490)
                         Joint contracture of the hand(HPO:0009473)
                            Camptodactyly of finger(HPO:0100490)
             Abnormal joint morphology(HPO:0001367)
                Abnormality of joint mobility(HPO:0011729)
                   Flexion contracture(HPO:0001371)
                      Camptodactyly(HPO:0012385)
                         Camptodactyly of finger(HPO:0100490)
                      Limb joint contracture(HPO:0003121)
                         Contractures of the joints of the upper limbs(HPO:0100360)
                            Joint contracture of the hand(HPO:0009473)
                               Camptodactyly of finger(HPO:0100490)
                Abnormality of upper limb joint(HPO:0009810)
                   Joint contracture of the hand(HPO:0009473)
                      Camptodactyly of finger(HPO:0100490)
MedDRA:
Database Frequency: 212 / 7739
Resource:

All diseases associated with this symptom:

15q24 microdeletion syndrome (Orphanet:94065)
16p11.2p12.2 microdeletion syndrome (Orphanet:261211)
16p13.11 microdeletion syndrome (Orphanet:261236)
1p36 deletion syndrome (Orphanet:1606)
2p15p16.1 microdeletion syndrome (Orphanet:261349)
2q31.1 microdeletion syndrome (Orphanet:251014)
6q25 microdeletion syndrome (Orphanet:251056)
8q21.11 microdeletion syndrome (Orphanet:284160)
8q22.1 microdeletion syndrome (Orphanet:178303)
ARTHROGRYPOSIS, DISTAL, TYPE 1A (OMIM:108120)
ARTHROGRYPOSIS, DISTAL, WITH HYPOPITUITARISM, MENTAL RETARDATION,AND FACIAL ANOMALIES (OMIM:208080)
Aarskog-Scott syndrome (Orphanet:915)
Aase-Smith syndrome (Orphanet:916)
Ablepharon macrostomia syndrome (Orphanet:920)
Absence of fingerprints - congenital milia (Orphanet:1658)
Acro-cardio-facial syndrome (Orphanet:2008)
Acro-fronto-facio-nasal dysostosis (Orphanet:1784)
Acropectorovertebral dysplasia (Orphanet:957)
Allan-Herndon-Dudley syndrome (Orphanet:59)
Anophthalmia - megalocornea - cardiopathy - skeletal anomalies (Orphanet:1101)
Antecubital pterygium syndrome (Orphanet:2987)
Antley-Bixler syndrome (Orphanet:83)
Aphalangy - syndactyly - microcephaly (Orphanet:1113)
Arthrogryposis with oculomotor limitation and electroretinal anomalies (Orphanet:1154)
Autism spectrum disorder-epilepsy-arthrogryposis syndrome (Orphanet:370943)
Autosomal dominant Robinow syndrome (Orphanet:3107)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Autosomal recessive multiple pterygium syndrome (Orphanet:2990)
Autosomal recessive palmoplantar keratoderma and congenital alopecia (Orphanet:1366)
Autosomal recessive spondylocostal dysostosis (Orphanet:2311)
Bethlem myopathy (Orphanet:610)
Blau syndrome (Orphanet:90340)
Blepharophimosis-intellectual deficit syndrome, SBBYS type (Orphanet:3047)
Bohring-Opitz syndrome (Orphanet:97297)
Bowen-Conradi syndrome (Orphanet:1270)
CEREBROOCULOFACIOSKELETAL SYNDROME 2 (OMIM:610756)
CEREBROOCULOFACIOSKELETAL SYNDROME 4 (OMIM:610758)
CHOLESTASIS WITH GALLSTONE, ATAXIA, AND VISUAL DISTURBANCE (OMIM:214980)
CHST3-related skeletal dysplasia (Orphanet:263463)
COFS syndrome (Orphanet:1466)
Camptobrachydactyly (Orphanet:1319)
Camptodactyly - fibrous tissue hyperplasia - skeletal dysplasia (Orphanet:1321)
Camptodactyly - joint contractures - facial skeletal defects (Orphanet:1323)
Camptodactyly - tall stature - scoliosis - hearing loss (Orphanet:85164)
Camptodactyly - taurinuria (Orphanet:1325)
Camptodactyly of fingers (Orphanet:295016)
Camptodactyly syndrome, Guadalajara type 1 (Orphanet:1327)
Camptodactyly syndrome, Guadalajara type 2 (Orphanet:1326)
Cardiocranial syndrome, Pfeiffer type (Orphanet:2872)
Carney complex-trismus-pseudocamptodactyly syndrome (Orphanet:319340)
Catel-Manzke syndrome (Orphanet:1388)
Coloboma of macula - brachydactyly type B (Orphanet:1471)
Congenital cataracts - facial dysmorphism - neuropathy (Orphanet:48431)
Congenital contractural arachnodactyly (Orphanet:115)
Cooper-Jabs syndrome (Orphanet:1488)
Craniofacial-deafness-hand syndrome (Orphanet:1529)
Craniofrontonasal dysplasia (Orphanet:1520)
DIGITOTALAR DYSMORPHISM (OMIM:126050)
Deafness - enamel hypoplasia - nail defects (Orphanet:3220)
Dermato-cardio-skeletal syndrome, Borrone type (Orphanet:1266)
Desbuquois syndrome (Orphanet:1425)
Diastrophic dwarfism (Orphanet:628)
Digitotalar dysmorphism (Orphanet:1146)
Distal 22q11.2 microdeletion syndrome (Orphanet:261330)
Distal 22q11.2 microduplication syndrome (Orphanet:261337)
Distal arthrogryposis type 10 (Orphanet:251515)
Distal symphalangism (Orphanet:3248)
Distal trisomy 15q (Orphanet:1707)
Distal trisomy 18q (Orphanet:1716)
Ear-patella-short stature syndrome (Orphanet:2554)
Ectodermal dysplasia - sensorineural deafness (Orphanet:1883)
Ectrodactyly - polydactyly (Orphanet:1892)
Ehlers-Danlos syndrome, spondylocheirodysplastic type (Orphanet:157965)
Emery-Nelson syndrome (Orphanet:1927)
Eng-Strom syndrome (Orphanet:1937)
Extensor tendons of finger anomalies (Orphanet:3294)
FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULARINVOLVEMENT (OMIM:600638)
Familial visceral myopathy (Orphanet:2604)
Fetal akinesia deformation sequence (Orphanet:994)
Fibrochondrogenesis (Orphanet:2021)
Fine-Lubinsky syndrome (Orphanet:1272)
Flat face - microstomia - ear anomaly (Orphanet:1968)
Floating-Harbor syndrome (Orphanet:2044)
Focal dermal hypoplasia (Orphanet:2092)
Freeman-Sheldon syndrome (Orphanet:2053)
Frontometaphyseal dysplasia (Orphanet:1826)
Frontonasal dysplasia (Orphanet:250)
GELEOPHYSIC DYSPLASIA 1 (OMIM:231050)
GM1 gangliosidosis (Orphanet:354)
Galloway-Mowat syndrome (Orphanet:2065)
Geleophysic dysplasia (Orphanet:2623)
German syndrome (Orphanet:2077)
Gordon syndrome (Orphanet:376)
HUNTER-MACDONALD SYNDROME (OMIM:611962)
Hennekam syndrome (Orphanet:2136)
Hennekam-Beemer syndrome (Orphanet:2135)
Hereditary acrokeratotic poikiloderma, Weary type (Orphanet:2907)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Hypertryptophanemia (Orphanet:2224)
Hypoplastic tibiae - postaxial polydactyly (Orphanet:3332)
Ichthyosis follicularis - alopecia - photophobia (Orphanet:2273)
Incontinentia pigmenti (Orphanet:464)
Intellectual deficit - athetosis - microphthalmia (Orphanet:1236)
Intellectual deficit - hypoplastic corpus callosum - preauricular tag (Orphanet:1495)
Intellectual deficit, Wolff type (Orphanet:3080)
Intellectual deficit, X-linked - seizures - psoriasis (Orphanet:3052)
Intellectual deficit, X-linked, Vitale type (Orphanet:85289)
Ito hypomelanosis (Orphanet:435)
Kapur-Toriello syndrome (Orphanet:2328)
Kindler syndrome (Orphanet:2908)
Leri pleonosteosis (Orphanet:2900)
Lethal multiple pterygium syndrome (Orphanet:33108)
Lethal restrictive dermopathy (Orphanet:1662)
Lichstenstein syndrome (Orphanet:2390)
Localized junctional epidermolysis bullosa, non-Herlitz type (Orphanet:251393)
Loeys-Dietz syndrome type 1 (Orphanet:60030)
MANDIBULOFACIAL DYSOSTOSIS WITH PTOSIS, AUTOSOMAL DOMINANT (OMIM:608257)
MASA syndrome (Orphanet:2466)
MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY (OMIM:259600)
MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET (OMIM:614399)
Malignant hyperthermia - arthrogryposis - torticollis (Orphanet:2215)
Marden-Walker syndrome (Orphanet:2461)
Mesomelic dwarfism - cleft palate - camptodactyly (Orphanet:2631)
Mesomelic dwarfism, Nievergelt type (Orphanet:2633)
Mesomelic dysplasia, Kantaputra type (Orphanet:1836)
Metaphyseal dysplasia - maxillary hypoplasia - brachydacty (Orphanet:2504)
Metatropic dysplasia (Orphanet:2635)
Microcephaly - cleft palate (Orphanet:2521)
Microphthalmia - microtia - fetal akinesia (Orphanet:2547)
Microphthalmia, Lenz type (Orphanet:568)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)
Morse-Rawnsley-Sargent syndrome (Orphanet:2570)
Mosaic trisomy 14 (Orphanet:1703)
Mosaic trisomy 15 (Orphanet:1706)
Mosaic trisomy 8 (Orphanet:96061)
Mosaic trisomy 9 (Orphanet:99776)
Mowat-Wilson syndrome (Orphanet:2152)
Muckle-Wells syndrome (Orphanet:575)
Multicentric carpo-tarsal osteolysis with or without nephropathy (Orphanet:2774)
Mutilating palmoplantar keratoderma with periorificial keratotic plaques (Orphanet:659)
Nakajo-Nishimura syndrome (Orphanet:2615)
Neurogenic arthrogryposis multiplex congenita (Orphanet:1143)
Oculocerebrorenal syndrome (Orphanet:534)
Oculodentodigital dysplasia (Orphanet:2710)
Oculomaxillofacial dysostosis (Orphanet:1794)
Oliver syndrome (Orphanet:2920)
Ophthalmomandibulomelic dysplasia (Orphanet:2741)
Orofaciodigital syndrome type 4 (Orphanet:2753)
Orofaciodigital syndrome type 8 (Orphanet:2755)
Osteopathia striata - cranial sclerosis (Orphanet:2780)
Otopalatodigital syndrome type 2 (Orphanet:90652)
PHAVER syndrome (Orphanet:2876)
Pentasomy X (Orphanet:11)
Polyneuropathy - hand defect (Orphanet:2926)
Polyneuropathy - intellectual deficit - acromicria - premature menopause (Orphanet:2928)
Polysyndactyly - cardiac malformation (Orphanet:2934)
Postaxial acrofacial dysostosis (Orphanet:246)
Progressive pseudorheumatoid arthropathy of childhood (Orphanet:1159)
Prominent glabella - microcephaly - hypogenitalism (Orphanet:2083)
Proximal symphalangism (Orphanet:3250)
Recombinant 8 syndrome (Orphanet:96167)
Retroperitoneal fibrosis (Orphanet:49041)
SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1 (OMIM:604320)
Say-Field-Coldwell syndrome (Orphanet:3133)
Scheie syndrome (Orphanet:93474)
Schinzel-Giedion syndrome (Orphanet:798)
Schwartz-Jampel syndrome (Orphanet:800)
Sheldon-Hall syndrome (Orphanet:1147)
Short stature - craniofacial anomalies - genital hypoplasia (Orphanet:2994)
Short stature - wormian bones - dextrocardia (Orphanet:2863)
Shprintzen-Goldberg syndrome (Orphanet:2462)
Sillence syndrome (Orphanet:3168)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Spinal muscular atrophy with respiratory distress (Orphanet:98920)
Spondylocamptodactyly syndrome (Orphanet:3180)
Stoll-Alembik-Finck syndrome (Orphanet:3200)
Stüve-Wiedemann syndrome (Orphanet:3206)
Syndactyly type 2 (Orphanet:93403)
Syndactyly type 3 (Orphanet:93404)
Syndactyly type 4 (Orphanet:93405)
Syndactyly type 5 (Orphanet:93406)
Syndromic X-linked intellectual deficit due to JARID1C mutation (Orphanet:85279)
Teebi-Shaltout syndrome (Orphanet:3291)
Tel Hashomer camptodactyly syndrome (Orphanet:3292)
Telecanthus - hypertelorism - strabismus - pes cavus (Orphanet:3293)
Terminal osseous dysplasia - pigmentary defects (Orphanet:88630)
Thoraco-abdominal enteric duplication (Orphanet:1759)
Thrombocytopenia - Robin sequence (Orphanet:3323)
Thumb deformity - alopecia - pigmentation anomaly (Orphanet:2251)
Toriello-Carey syndrome (Orphanet:3338)
Tricho-oculo-dermo-vertebral syndrome (Orphanet:3354)
Trichorhinophalangeal syndrome type 1 and 3 (Orphanet:77258)
Trisomy 18 (Orphanet:3380)
Trisomy 1q (Orphanet:261344)
Trisomy 20p (Orphanet:261318)
Trisomy 4p (Orphanet:1738)
Trisomy 8q (Orphanet:1752)
URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME (OMIM:300280)
Ulnar-mammary syndrome (Orphanet:3138)
Urban-Rogers-Meyer syndrome (Orphanet:3409)
Van den Ende-Gupta syndrome (Orphanet:2460)
Ventricular extrasystoles with syncopal episodes - perodactyly - Robin sequence (Orphanet:3201)
W syndrome (Orphanet:2804)
WT limb-blood syndrome (Orphanet:3466)
Waardenburg syndrome (Orphanet:3440)
Waardenburg syndrome type 3 (Orphanet:896)
Weaver syndrome (Orphanet:3447)
X-linked distal arthrogryposis multiplex congenita (Orphanet:1145)
X-linked intellectual deficit - hypotonic face (Orphanet:73220)
X-linked intellectual deficit with marfanoid habitus (Orphanet:776)
Zellweger-like syndrome without peroxisomal anomalies (Orphanet:50812)