Preaxial hand polydactyly

Symptom Information:

Symptom ID: HPO:0001177
Synonyms:
Polydactyly affecting the thumb [HPO:0001177]
Polydactyly, preaxial [HPO:0001177]
Preaxial polydactyly (hands) [HPO:0001177]
thumb polydactyly [HPO:0001177]
Preaxial polydactyly of hand [Orphanet:20500]
Radial polydactyly [HPO:0001177]
Radial polydactyly (disorder) [Orphanet:20500]
Radial polydactyly [Orphanet:20500]
Polydactyly, preaxial [OMIM:Polydactyly, preaxial]
Thumb polydactyly [OMIM:Thumb polydactyly]
Preaxial polydactyly (hand) [Orphanet:20500]
Polydactyly, preaxial (rare) [OMIM:Polydactyly, preaxial (rare)]
Preaxial polydactyly (rare) [OMIM:Preaxial polydactyly (rare)]
Preaxial polydactyly (variable) [OMIM:Preaxial polydactyly (variable)]
Quality:
Cross references:
Orphanet:20500 "Preaxial polydactyly (hand)" [Orphanet:20500]
OMIM: "Polydactyly, preaxial" [OMIM:Polydactyly, preaxial]
OMIM: "Thumb polydactyly" [OMIM:Thumb polydactyly]
OMIM: "Polydactyly, preaxial (rare)" [OMIM:Polydactyly, preaxial (rare)]
OMIM: "Preaxial polydactyly (rare)" [OMIM:Preaxial polydactyly (rare)]
OMIM: "Preaxial polydactyly (variable)" [OMIM:Preaxial polydactyly (variable)]
UMLS:C0345354 "Radial polydactyly" [Orphanet:20500]
Is a (Direct Parents):
HPO         Hand polydactyly
HPO         Preaxial polydactyly
Orphanet Hand polydactyly
HPO         Abnormality of the thumb
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 digit(HPO:0011297)
                      Polydactyly(HPO:0010442)
                         Preaxial polydactyly(HPO:0100258)
                            Preaxial hand polydactyly(HPO:0001177)
                         Hand polydactyly(HPO:0001161)
                            Preaxial hand polydactyly(HPO:0001177)
                      Abnormality of finger(HPO:0001167)
                         Abnormality of the thumb(HPO:0001172)
                            Preaxial hand polydactyly(HPO:0001177)
                         Abnormality of phalanx of finger(HPO:0005918)
                            Duplication of phalanx of hand(HPO:0009997)
                               Hand polydactyly(HPO:0001161)
                                  Preaxial hand polydactyly(HPO:0001177)
                   Abnormality of the upper limb(HPO:0002817)
                      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)
                                  Preaxial hand polydactyly(HPO:0001177)
                      Abnormality of the hand(HPO:0001155)
                         Duplication of hand bones(HPO:0004275)
                            Duplication of phalanx of hand(HPO:0009997)
                               Hand polydactyly(HPO:0001161)
                                  Preaxial hand polydactyly(HPO:0001177)
                         Abnormality of finger(HPO:0001167)
                            Abnormality of the thumb(HPO:0001172)
                               Preaxial hand polydactyly(HPO:0001177)
                            Abnormality of phalanx of finger(HPO:0005918)
                               Duplication of phalanx of hand(HPO:0009997)
                                  Hand polydactyly(HPO:0001161)
                                     Preaxial hand polydactyly(HPO:0001177)
MedDRA:
Database Frequency: 59 / 7739
Resource:

All diseases associated with this symptom:

Acro-pectoral syndrome (Orphanet:85203)
Acro-renal-ocular syndrome (Orphanet:959)
Acrocallosal syndrome (Orphanet:36)
Apert syndrome (Orphanet:87)
Biemond syndrome type 2 (Orphanet:141333)
Bowed tibiae - radial anomalies - osteopenia - fractures (Orphanet:3331)
Brachydactyly - preaxial hallux varus (Orphanet:1278)
Braddock syndrome (Orphanet:52047)
Branchio-oculo-facial syndrome (Orphanet:1297)
CERVICAL RIBS, SPRENGEL ANOMALY, ANAL ATRESIA, AND URETHRAL OBSTRUCTION (OMIM:601389)
CHARGE syndrome (Orphanet:138)
Curry-Jones syndrome (Orphanet:1553)
Diabetic embryopathy (Orphanet:1926)
Femoral-facial syndrome (Orphanet:1988)
Greig cephalopolysyndactyly syndrome (Orphanet:380)
Hallux varus - preaxial polysyndactyly (Orphanet:2110)
Hydrolethalus (Orphanet:2189)
Hypertelorism - hypospadias - polysyndactyly syndrome (Orphanet:2211)
Hypoplastic tibiae - postaxial polydactyly (Orphanet:3332)
IVIC syndrome (Orphanet:2307)
Intellectual deficit, X-linked, Siderius type (Orphanet:85287)
Joubert syndrome with orofaciodigital defect (Orphanet:2754)
Lacrimo-auriculo-dento-digital syndrome (Orphanet:2363)
Laurin-Sandrow syndrome (Orphanet:2378)
Lung agenesis - heart defect - thumb anomalies (Orphanet:1120)
MENTAL RETARDATION, MICROCEPHALY, GROWTH RETARDATION, JOINT CONTRACTURES,AND FACIAL DYSMORPHISM (OMIM:606242)
MICROCEPHALY, CORPUS CALLOSUM DYSGENESIS, AND CLEFT LIP/PALATE (OMIM:601420)
Mandibulofacial dysostosis-microcephaly syndrome (Orphanet:79113)
Meckel syndrome (Orphanet:564)
Microphthalmia with brain and digit anomalies (Orphanet:139471)
Neuroectodermal syndrome, Johnson type (Orphanet:2316)
Oculoauriculovertebral spectrum with radial defects (Orphanet:2549)
Oculodentodigital dysplasia (Orphanet:2710)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Orofaciodigital syndrome type 10 (Orphanet:2756)
Orofaciodigital syndrome type 2 (Orphanet:2751)
Orofaciodigital syndrome type 4 (Orphanet:2753)
Orofaciodigital syndrome type 5 (Orphanet:2919)
Polydactyly of a biphalangeal thumb (Orphanet:93339)
Polysyndactyly - cardiac malformation (Orphanet:2934)
Preaxial polydactyly - colobomata - intellectual deficit (Orphanet:2921)
Preaxial polydactyly of toes (Orphanet:295006)
Rhizomelic syndrome, Urbach type (Orphanet:3098)
Sakati-Nyhan syndrome (Orphanet:3128)
Say-Field-Coldwell syndrome (Orphanet:3133)
Short rib-polydactyly syndrome (Orphanet:1505)
Short rib-polydactyly syndrome, Majewski type (Orphanet:93269)
Short rib-polydactyly syndrome, Verma-Naumoff type (Orphanet:93271)
Syndactyly-polydactyly-ear lobe syndrome (Orphanet:3259)
Synpolydactyly type 1 (Orphanet:295195)
Thalidomide embryopathy (Orphanet:3312)
Tibial aplasia - ectrodactyly (Orphanet:3329)
Townes-Brocks syndrome (Orphanet:857)
Triphalangeal thumb - polysyndactyly syndrome (Orphanet:2950)
Trisomy 1q (Orphanet:261344)
Trisomy 20p (Orphanet:261318)
Trisomy 4p (Orphanet:1738)
VACTERL/VATER association (Orphanet:887)
Wolf-Hirschhorn syndrome (Orphanet:280)