Hand polydactyly

Symptom Information:

Symptom ID: HPO:0001161
Synonyms:
Polydactyly (hands) [HPO:0001161]
Polydactyly of fingers [HPO:0001161]
Polydactyly of fingers (disorder) [Orphanet:20480]
Hand polydactyly [Orphanet:20480]
Upper limb polydactyly/hexadactyly [Orphanet:20480]
Polydactyly of fingers [Orphanet:20480]
Polydactyly [MedDRA:10036063]
Multiple digits [MedDRA:10036063]
Polydactyly of fingers [MedDRA:10036063]
Polydactyly of toes [MedDRA:10036063]
Polydactyly, unspecified digits [MedDRA:10036063]
Polydactyly (homozygote) [OMIM:Polydactyly (homozygote)]
Polydactyly (in 1 patient) [OMIM:Polydactyly (in 1 patient)]
Polydactyly (in some patients) [OMIM:Polydactyly (in some patients)]
Polydactyly (in some) [OMIM:Polydactyly (in some)]
Polydactyly (major) [OMIM:Polydactyly (major)]
Polydactyly (rare) [OMIM:Polydactyly (rare)]
Polydactyly (variable) [OMIM:Polydactyly (variable)]
Quality:
Cross references:
Orphanet:20480 "Upper limb polydactyly/hexadactyly" [Orphanet:20480]
OMIM: "Polydactyly (homozygote)" [OMIM:Polydactyly (homozygote)]
OMIM: "Polydactyly (in 1 patient)" [OMIM:Polydactyly (in 1 patient)]
OMIM: "Polydactyly (in some patients)" [OMIM:Polydactyly (in some patients)]
OMIM: "Polydactyly (in some)" [OMIM:Polydactyly (in some)]
OMIM: "Polydactyly (major)" [OMIM:Polydactyly (major)]
OMIM: "Polydactyly (rare)" [OMIM:Polydactyly (rare)]
OMIM: "Polydactyly (variable)" [OMIM:Polydactyly (variable)]
UMLS:C0158733 "Hand polydactyly" [Orphanet:20480]
Is a (Direct Parents):
HPO         Duplication of phalanx of hand
MedDRA Musculoskeletal and connective tissue disorders of limbs congenital
HPO         Polydactyly
Orphanet Abnormality of the hand
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)
                         Duplication of hand bones(HPO:0004275)
                            Duplication of phalanx of hand(HPO:0009997)
                               Hand polydactyly(HPO:0001161)
                         Abnormality of finger(HPO:0001167)
                            Abnormality of phalanx of finger(HPO:0005918)
                               Duplication of phalanx of hand(HPO:0009997)
                                  Hand polydactyly(HPO:0001161)
                      Duplication of bones involving the upper extremities(HPO:0009142)
                         Duplication of hand bones(HPO:0004275)
                            Duplication of phalanx of hand(HPO:0009997)
                               Hand polydactyly(HPO:0001161)
                   Abnormality of digit(HPO:0011297)
                      Polydactyly(HPO:0010442)
                         Hand polydactyly(HPO:0001161)
                      Abnormality of finger(HPO:0001167)
                         Abnormality of phalanx of finger(HPO:0005918)
                            Duplication of phalanx of hand(HPO:0009997)
                               Hand polydactyly(HPO:0001161)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Musculoskeletal and connective tissue disorders congenital(MedDRA:10028396)
       Musculoskeletal and connective tissue disorders of limbs congenital(MedDRA:10028381)
          Hand polydactyly(HPO:0001161)
Database Frequency: 71 / 7739
Resource:

All diseases associated with this symptom:

16p13.11 microduplication syndrome (Orphanet:261243)
1p36 deletion syndrome (Orphanet:1606)
1q21.1 microdeletion syndrome (Orphanet:250989)
22q11.2 deletion syndrome (Orphanet:567)
3C syndrome (Orphanet:7)
Absent tibia - polydactyly (Orphanet:988)
Acro-pectoro-renal dysplasia (Orphanet:956)
Acro-renal-mandibular syndrome (Orphanet:958)
Acrocephalopolydactyly (Orphanet:221054)
Angio-osteohypertrophic syndrome (Orphanet:2346)
Antecubital pterygium syndrome (Orphanet:2987)
Bardet-Biedl syndrome (Orphanet:110)
Bardet-Biedl syndrome 12 (OMIM:615989)
Bardet-Biedl syndrome 2 (OMIM:615981)
Bardet-Biedl syndrome 4 (OMIM:615982)
Bardet-Biedl syndrome 7 (OMIM:615984)
Bardet-Biedl syndrome 9 (OMIM:615986)
Bloom syndrome (Orphanet:125)
C syndrome (Orphanet:1308)
CHARGE syndrome (Orphanet:138)
Camptobrachydactyly (Orphanet:1319)
Char syndrome (Orphanet:46627)
Constriction rings syndrome (Orphanet:295000)
Craniofrontonasal dysplasia (Orphanet:1520)
DISORGANIZATION, MOUSE, HOMOLOG OF (OMIM:223200)
Diabetic embryopathy (Orphanet:1926)
EEC syndrome (Orphanet:1896)
Ectodermal dysplasia syndrome (Orphanet:79373)
Ellis Van Creveld syndrome (Orphanet:289)
Focal dermal hypoplasia (Orphanet:2092)
Goodman syndrome (Orphanet:65798)
Gorlin syndrome (Orphanet:377)
Harlequin ichthyosis (Orphanet:457)
Heart-hand syndrome type 2 (Orphanet:1350)
Hidrotic ectodermal dysplasia (Orphanet:189)
Hirschsprung disease - deafness - polydactyly (Orphanet:2155)
Holoprosencephaly (Orphanet:2162)
Holzgreve-Wagner-Rehder syndrome (Orphanet:2167)
Hypertelorism - hypospadias - polysyndactyly syndrome (Orphanet:2211)
Ito hypomelanosis (Orphanet:435)
Jacobsen syndrome (Orphanet:2308)
Jeune syndrome (Orphanet:474)
Joubert syndrome (Orphanet:475)
Joubert syndrome 15 (OMIM:614464)
Joubert syndrome 16 (OMIM:614465)
Joubert syndrome 17 (OMIM:614615)
Joubert syndrome with ocular defect (Orphanet:220493)
Joubert syndrome with oculorenal defect (Orphanet:2318)
Joubert syndrome with orofaciodigital defect (Orphanet:2754)
Joubert syndrome with renal defect (Orphanet:220497)
Laurence-Moon syndrome (Orphanet:2377)
Laurin-Sandrow syndrome (Orphanet:2378)
MESOAXIAL HEXADACTYLY AND CARDIAC MALFORMATION (OMIM:249670)
Megalencephaly-capillary malformation-polymicrogyria syndrome (Orphanet:60040)
Microphthalmia with limb anomalies (Orphanet:1106)
Nephronophthisis 15 (OMIM:614845)
Neuroectodermal syndrome, Johnson type (Orphanet:2316)
Oculocerebrocutaneous syndrome (Orphanet:1647)
Oculodentodigital dysplasia (Orphanet:2710)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Orofaciodigital syndrome type 9 (Orphanet:141007)
Otopalatodigital syndrome (Orphanet:669)
PELGER-HUET ANOMALY (OMIM:169400)
Peroxisomal acyl-CoA oxidase deficiency (Orphanet:2971)
Proximal 16p11.2 microdeletion syndrome (Orphanet:261197)
SHORT syndrome (Orphanet:3163)
Schinzel-Giedion syndrome (Orphanet:798)
Smith-Magenis syndrome (Orphanet:819)
Syndactyly type 4 (Orphanet:93405)
Syndrome with brachydactyly (Orphanet:69028)
VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS (OMIM:314390)