Postaxial hand polydactyly

Symptom Information:

Symptom ID: HPO:0001162
Synonyms:
Polydactyly affecting the 5th finger [HPO:0001162]
Polydactyly, postaxial [HPO:0001162]
Postaxial polydactyly (hands) [HPO:0001162]
Postaxial polydactyly of fingers [HPO:0001162]
Postaxial polydactyly of hand [HPO:0001162]
Postaxial polydactyly of hands [HPO:0001162]
Postaxial polydactyly of hand [Orphanet:20520]
Polydactyly, postaxial [OMIM:Polydactyly, postaxial]
Postaxial polydactyly of hand [OMIM:Postaxial polydactyly of hand]
Postaxial polydactyly of hands [OMIM:Postaxial polydactyly of hands]
Postaxial polydactyly (hand) [Orphanet:20520]
Polydactyly, postaxial (less common) [OMIM:Polydactyly, postaxial (less common)]
Polydactyly, postaxial (rare) [OMIM:Polydactyly, postaxial (rare)]
Postaxial polydactyly (1 fetus) [OMIM:Postaxial polydactyly (1 fetus)]
Postaxial polydactyly (1 patient) [OMIM:Postaxial polydactyly (1 patient)]
Postaxial polydactyly (in some patients) [OMIM:Postaxial polydactyly (in some patients)]
Postaxial polydactyly (rare) [OMIM:Postaxial polydactyly (rare)]
Quality:
Cross references:
Orphanet:20520 "Postaxial polydactyly (hand)" [Orphanet:20520]
OMIM: "Polydactyly, postaxial" [OMIM:Polydactyly, postaxial]
OMIM: "Postaxial polydactyly of hand" [OMIM:Postaxial polydactyly of hand]
OMIM: "Postaxial polydactyly of hands" [OMIM:Postaxial polydactyly of hands]
OMIM: "Polydactyly, postaxial (less common)" [OMIM:Polydactyly, postaxial (less common)]
OMIM: "Polydactyly, postaxial (rare)" [OMIM:Polydactyly, postaxial (rare)]
OMIM: "Postaxial polydactyly (1 fetus)" [OMIM:Postaxial polydactyly (1 fetus)]
OMIM: "Postaxial polydactyly (1 patient)" [OMIM:Postaxial polydactyly (1 patient)]
OMIM: "Postaxial polydactyly (in some patients)" [OMIM:Postaxial polydactyly (in some patients)]
OMIM: "Postaxial polydactyly (rare)" [OMIM:Postaxial polydactyly (rare)]
Is a (Direct Parents):
Orphanet Hand polydactyly
HPO         Postaxial polydactyly
HPO         Abnormality of the 5th finger
HPO         Hand polydactyly
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)
                         Hand polydactyly(HPO:0001161)
                            Postaxial hand polydactyly(HPO:0001162)
                         Postaxial polydactyly(HPO:0100259)
                            Postaxial hand polydactyly(HPO:0001162)
                      Abnormality of finger(HPO:0001167)
                         Abnormality of the 5th finger(HPO:0004207)
                            Postaxial hand polydactyly(HPO:0001162)
                         Abnormality of phalanx of finger(HPO:0005918)
                            Duplication of phalanx of hand(HPO:0009997)
                               Hand polydactyly(HPO:0001161)
                                  Postaxial hand polydactyly(HPO:0001162)
                   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)
                                  Postaxial hand polydactyly(HPO:0001162)
                      Abnormality of the hand(HPO:0001155)
                         Duplication of hand bones(HPO:0004275)
                            Duplication of phalanx of hand(HPO:0009997)
                               Hand polydactyly(HPO:0001161)
                                  Postaxial hand polydactyly(HPO:0001162)
                         Abnormality of finger(HPO:0001167)
                            Abnormality of the 5th finger(HPO:0004207)
                               Postaxial hand polydactyly(HPO:0001162)
                            Abnormality of phalanx of finger(HPO:0005918)
                               Duplication of phalanx of hand(HPO:0009997)
                                  Hand polydactyly(HPO:0001161)
                                     Postaxial hand polydactyly(HPO:0001162)
MedDRA:
Database Frequency: 119 / 7739
Resource:

All diseases associated with this symptom:

Absent tibia - polydactyly - arachnoid cyst (Orphanet:3328)
Acalvaria (Orphanet:945)
Achondrogenesis type 2 (Orphanet:93296)
Acrocallosal syndrome (Orphanet:36)
Acrocephalopolydactyly (Orphanet:221054)
Acrofacial dysostosis, Weyers type (Orphanet:952)
Acromesomelic dysplasia, Grebe type (Orphanet:2098)
Apert syndrome (Orphanet:87)
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA (OMIM:609945)
BRESEK syndrome (Orphanet:85284)
Bardet-Biedl syndrome (Orphanet:110)
Bardet-Biedl syndrome 10 (OMIM:615987)
Bardet-Biedl syndrome 17 (OMIM:615994)
Bardet-Biedl syndrome 3 (OMIM:600151)
Bardet-Biedl syndrome 4 (OMIM:615982)
Beckwith-Wiedemann syndrome due to 11p15 microduplication (Orphanet:96076)
Brachydactyly - nystagmus - cerebellar ataxia (Orphanet:1246)
Brain malformation - congenital heart disease - postaxial polydactyly (Orphanet:75389)
C syndrome (Orphanet:1308)
CARPENTER SYNDROME 2 (OMIM:614976)
CONE-ROD DYSTROPHY 16 (OMIM:614500)
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl (OMIM:614576)
Carpenter syndrome (Orphanet:65759)
Cerebro-facio-thoracic dysplasia (Orphanet:1394)
Cerebro-oculo-nasal syndrome (Orphanet:66625)
Cortical blindness - intellectual deficit - polydactyly (Orphanet:1389)
Crossed polysyndactyly (Orphanet:2935)
Dandy-Walker malformation - postaxial polydactyly (Orphanet:1566)
Distal monosomy 3p (Orphanet:1620)
EVC2 GENE (OMIM:607261)
Ectrodactyly - polydactyly (Orphanet:1892)
Ellis Van Creveld syndrome (Orphanet:289)
Focal dermal hypoplasia (Orphanet:2092)
Frontonasal dysplasia (Orphanet:250)
Fuhrmann syndrome (Orphanet:2854)
Genito-palato-cardiac syndrome (Orphanet:2075)
Greenberg dysplasia (Orphanet:1426)
Greig cephalopolysyndactyly syndrome (Orphanet:380)
Guttmacher syndrome (Orphanet:2957)
HOLOPROSENCEPHALY 9 (OMIM:610829)
HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED (OMIM:241800)
Hand-foot-genital syndrome (Orphanet:2438)
Heart defect - tongue hamartoma - polysyndactyly (Orphanet:1338)
Hirschsprung disease - deafness - polydactyly (Orphanet:2155)
Holoprosencephaly - postaxial polydactyly (Orphanet:2166)
Hydrolethalus (Orphanet:2189)
Hypoplastic tibiae - postaxial polydactyly (Orphanet:3332)
Ichthyosis follicularis - alopecia - photophobia (Orphanet:2273)
Intellectual deficit - polydactyly - uncombable hair (Orphanet:3082)
Jeune syndrome (Orphanet:474)
Joubert syndrome (Orphanet:475)
Joubert syndrome 1 (OMIM:213300)
Joubert syndrome 2 (OMIM:608091)
Joubert syndrome 20 (OMIM:614970)
Joubert syndrome 22 (OMIM:615665)
Joubert syndrome with hepatic defect (Orphanet:1454)
Joubert syndrome with oculorenal defect (Orphanet:2318)
KBG syndrome (Orphanet:2332)
LOEYS-DIETZ SYNDROME 1 (OMIM:609192)
LOEYS-DIETZ SYNDROME 2 (OMIM:610168)
Lathosterolosis (Orphanet:46059)
Lethal Larsen-like syndrome (Orphanet:2371)
Loeys-Dietz syndrome type 1 (Orphanet:60030)
MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 2 (OMIM:615937)
MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 3 (OMIM:615938)
McKusick-Kaufman syndrome (Orphanet:2473)
Meckel syndrome (Orphanet:564)
Meckel syndrome, type 2 (OMIM:603194)
Meckel syndrome, type 3 (OMIM:607361)
Meckel syndrome, type 4 (OMIM:611134)
Meckel syndrome, type 5 (OMIM:611561)
Meckel syndrome, type 6 (OMIM:612284)
Meckel syndrome, type 8 (OMIM:613885)
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus (Orphanet:83473)
Microcephaly - seizures - intellectual deficit - heart disease (Orphanet:2519)
Microphthalmia with limb anomalies (Orphanet:1106)
Monosomy 9p (Orphanet:261112)
Mullerian derivatives - lymphangiectasia - polydactyly (Orphanet:1655)
Mullerian duct anomalies - limb anomalies (Orphanet:2491)
Multinodular goiter - cystic kidney - polydactyly (Orphanet:2091)
Non-distal trisomy 13q (Orphanet:1702)
Non-rhizomelic chondrodysplasia punctata (Orphanet:176)
Oliver syndrome (Orphanet:2920)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Orofaciodigital syndrome type 2 (Orphanet:2751)
Orofaciodigital syndrome type 3 (Orphanet:2752)
Orofaciodigital syndrome type 4 (Orphanet:2753)
Orofaciodigital syndrome type 5 (Orphanet:2919)
Orofaciodigital syndrome type 8 (Orphanet:2755)
Otopalatodigital syndrome (Orphanet:669)
POLYDACTYLY, POSTAXIAL, TYPE A2 (OMIM:602085)
POLYDACTYLY, POSTAXIAL, TYPE A5 (OMIM:263450)
POLYDACTYLY, POSTAXIAL, TYPE A6 (OMIM:615226)
Pallister-Hall syndrome (Orphanet:672)
Polydactyly-myopia syndrome (Orphanet:2917)
Polysyndactyly - cardiac malformation (Orphanet:2934)
Postaxial polydactyly - dental and vertebral anomalies (Orphanet:2916)
Postaxial polydactyly type A (Orphanet:93334)
Postaxial tetramelic oligodactyly (Orphanet:2730)
Scalp defects - postaxial polydactyly (Orphanet:1003)
Schinzel-Giedion syndrome (Orphanet:798)
Short rib-polydactyly syndrome (Orphanet:1505)
Short rib-polydactyly syndrome, Majewski type (Orphanet:93269)
Short rib-polydactyly syndrome, Verma-Naumoff type (Orphanet:93271)
Short-rib thoracic dysplasia 10 with or without polydactyly (OMIM:615630)
Short-rib thoracic dysplasia 2 with or without polydactyly (OMIM:611263)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Syndactyly type 2 (Orphanet:93403)
Syndactyly-polydactyly-ear lobe syndrome (Orphanet:3259)
THAI SYMPHALANGISM SYNDROME (OMIM:608028)
Tetrasomy 12p (Orphanet:884)
Tibial aplasia - ectrodactyly (Orphanet:3329)
Triphalangeal thumb - polysyndactyly syndrome (Orphanet:2950)
Trisomy 13 (Orphanet:3378)
Trisomy 18 (Orphanet:3380)
Ulnar-mammary syndrome (Orphanet:3138)
VENTRICULOMEGALY WITH CYSTIC KIDNEY DISEASE (OMIM:219730)
X-linked dominant chondrodysplasia punctata (Orphanet:35173)