Postaxial polydactyly

Symptom Information:

Symptom ID: HPO:0100259
Synonyms:
Postaxial hexadactyly [HPO:0100259]
Postaxial hexadactyly [OMIM:Postaxial hexadactyly]
Postaxial polydactyly [OMIM:Postaxial polydactyly]
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:
OMIM: "Postaxial hexadactyly" [OMIM:Postaxial hexadactyly]
OMIM: "Postaxial polydactyly" [OMIM:Postaxial polydactyly]
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):
HPO         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)
                         Postaxial polydactyly(HPO:0100259)
MedDRA:
Database Frequency: 85 / 7739
Resource:

All diseases associated with this symptom:

ARIMA SYNDROME (OMIM:243910)
Acrofacial dysostosis, Weyers type (Orphanet:952)
Acromesomelic dysplasia, Grebe type (Orphanet:2098)
Apert syndrome (Orphanet:87)
BRESEK syndrome (Orphanet:85284)
Bardet-Biedl syndrome (Orphanet:110)
Bardet-Biedl syndrome 12 (OMIM:615989)
Bardet-Biedl syndrome 17 (OMIM:615994)
Bardet-Biedl syndrome 2 (OMIM:615981)
Bardet-Biedl syndrome 3 (OMIM:600151)
Bardet-Biedl syndrome 5 (OMIM:615983)
Bardet-Biedl syndrome 6 (OMIM:605231)
C syndrome (Orphanet:1308)
CARPENTER SYNDROME 1 (OMIM:201000)
CARPENTER SYNDROME 2 (OMIM:614976)
CEREBELLAR VERMIS APLASIA WITH ASSOCIATED FEATURES SUGGESTING SMITH-LEMLI-OPITZSYNDROME AND MECKEL SYNDROME (OMIM:213010)
CONE-ROD DYSTROPHY 16 (OMIM:614500)
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl (OMIM:614576)
CULLER-JONES SYNDROME (OMIM:615849)
Cerebro-facio-thoracic dysplasia (Orphanet:1394)
Cerebro-oculo-nasal syndrome (Orphanet:66625)
Conotruncal heart malformations (Orphanet:2445)
Dandy-Walker malformation - postaxial polydactyly (Orphanet:1566)
Distal monosomy 3p (Orphanet:1620)
Ectrodactyly - polydactyly (Orphanet:1892)
Ellis Van Creveld syndrome (Orphanet:289)
Endocrine-cerebro-osteodysplasia syndrome (Orphanet:199332)
Focal dermal hypoplasia (Orphanet:2092)
Fuhrmann syndrome (Orphanet:2854)
Greig cephalopolysyndactyly syndrome (Orphanet:380)
HYDROLETHALUS SYNDROME 1 (OMIM:236680)
HYDROLETHALUS SYNDROME 2 (OMIM:614120)
HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED (OMIM:241800)
Heart defect - tongue hamartoma - polysyndactyly (Orphanet:1338)
Holoprosencephaly - postaxial polydactyly (Orphanet:2166)
Ichthyosis follicularis - alopecia - photophobia (Orphanet:2273)
Joubert syndrome 1 (OMIM:213300)
Joubert syndrome 10 (OMIM:300804)
Joubert syndrome 14 (OMIM:614424)
Joubert syndrome 20 (OMIM:614970)
Joubert syndrome 7 (OMIM:611560)
Joubert syndrome with orofaciodigital defect (Orphanet:2754)
LOEYS-DIETZ SYNDROME 1 (OMIM:609192)
LOEYS-DIETZ SYNDROME 2 (OMIM:610168)
Lathosterolosis (Orphanet:46059)
MICROPHTHALMIA, ISOLATED 4 (OMIM:613094)
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7 (OMIM:615824)
McKusick-Kaufman syndrome (Orphanet:2473)
Meckel syndrome, type 1 (OMIM:249000)
Meckel syndrome, type 10 (OMIM:614175)
Meckel syndrome, type 4 (OMIM:611134)
Meckel syndrome, type 5 (OMIM:611561)
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus (Orphanet:83473)
Microphthalmia with limb anomalies (Orphanet:1106)
Mullerian derivatives - lymphangiectasia - polydactyly (Orphanet:1655)
Mullerian duct anomalies - limb anomalies (Orphanet:2491)
OROFACIODIGITAL SYNDROME XIV (OMIM:615948)
Oliver syndrome (Orphanet:2920)
Orofaciodigital syndrome type 3 (Orphanet:2752)
Orofaciodigital syndrome type 5 (Orphanet:2919)
Otopalatodigital syndrome type 2 (Orphanet:90652)
POLYDACTYLY, POSTAXIAL, TYPE A2 (OMIM:602085)
Pallister-Hall syndrome (Orphanet:672)
Polydactyly-myopia syndrome (Orphanet:2917)
Postaxial polydactyly - dental and vertebral anomalies (Orphanet:2916)
Postaxial polydactyly type B (Orphanet:93335)
Postaxial tetramelic oligodactyly (Orphanet:2730)
SANTOS SYNDROME (OMIM:613005)
SHORT RIB-POLYDACTYLY SYNDROME, TYPE IIB (OMIM:615087)
Schinzel-Giedion syndrome (Orphanet:798)
Short rib-polydactyly syndrome, Saldino-Noonan type (Orphanet:93270)
Short-rib thoracic dysplasia 11 with or without polydactyly (OMIM:615633)
Short-rib thoracic dysplasia 3 with or without polydactyly (OMIM:613091)
Short-rib thoracic dysplasia 6 with or without polydactyly (OMIM:263520)
Short-rib thoracic dysplasia 7 with or without polydactyly (OMIM:614091)
Short-rib thoracic dysplasia 8 with or without polydactyly (OMIM:615503)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Synpolydactyly type 1 (Orphanet:295195)
TARP syndrome (Orphanet:2886)
THAI SYMPHALANGISM SYNDROME (OMIM:608028)
Tetrasomy 12p (Orphanet:884)
Ulnar-mammary syndrome (Orphanet:3138)
VENTRICULOMEGALY WITH CYSTIC KIDNEY DISEASE (OMIM:219730)
X-linked dominant chondrodysplasia punctata (Orphanet:35173)