Symptom Information:

Symptom ID: HPO:0010442
polydactyly [HPO:0010442]
Polydactyly [OMIM:Polydactyly]
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)]
Cross references:
OMIM: "Polydactyly" [OMIM:Polydactyly]
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:C2117329 "polydactyly" [HPO:0010442]
Is a (Direct Parents):
HPO         Abnormality of digit
Is a (Whole tree): HPO:
    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)
Database Frequency: 69 / 7739

All diseases associated with this symptom:

3C syndrome (Orphanet:7)
Absent tibia - polydactyly (Orphanet:988)
Acro-renal-mandibular syndrome (Orphanet:958)
Acrocephalopolydactyly (Orphanet:221054)
Bardet-Biedl syndrome (Orphanet:110)
Bardet-Biedl syndrome 1 (OMIM:209900 )
Bardet-Biedl syndrome 10 (OMIM:615987)
Bardet-Biedl syndrome 11 (OMIM:615988)
Bardet-Biedl syndrome 12 (OMIM:615989)
Bardet-Biedl syndrome 13 (OMIM:615990)
Bardet-Biedl syndrome 19 (OMIM:615996)
Bardet-Biedl syndrome 2 (OMIM:615981)
Bardet-Biedl syndrome 3 (OMIM:600151)
Bardet-Biedl syndrome 4 (OMIM:615982)
Bardet-Biedl syndrome 5 (OMIM:615983)
Bardet-Biedl syndrome 6 (OMIM:605231)
Bardet-Biedl syndrome 7 (OMIM:615984)
Bardet-Biedl syndrome 8 (OMIM:615985)
Bardet-Biedl syndrome 9 (OMIM:615986)
Beckwith-Wiedemann syndrome due to CDKN1C mutation (Orphanet:231120)
Bloom syndrome (Orphanet:125)
Brachydactyly type C (Orphanet:93384)
Branchio-oculo-facial syndrome (Orphanet:1297)
Camptobrachydactyly (Orphanet:1319)
Constriction rings syndrome (Orphanet:295000)
Diabetic embryopathy (Orphanet:1926)
Ectrodactyly - polydactyly (Orphanet:1892)
Focal dermal hypoplasia (Orphanet:2092)
Goodman syndrome (Orphanet:65798)
Gorlin syndrome (Orphanet:377)
Greenberg dysplasia (Orphanet:1426)
Hirschsprung disease - deafness - polydactyly (Orphanet:2155)
Holzgreve-Wagner-Rehder syndrome (Orphanet:2167)
Hypertelorism - hypospadias - polysyndactyly syndrome (Orphanet:2211)
Hypoplastic tibiae - postaxial polydactyly (Orphanet:3332)
Ito hypomelanosis (Orphanet:435)
Joubert syndrome 15 (OMIM:614464)
Joubert syndrome 16 (OMIM:614465)
Joubert syndrome 17 (OMIM:614615)
Joubert syndrome 18 (OMIM:614815)
Joubert syndrome 2 (OMIM:608091)
Joubert syndrome 22 (OMIM:615665)
Joubert syndrome 28 (OMIM:617121)
Klippel-Trénaunay syndrome (Orphanet:90308)
Meckel syndrome, type 1 (OMIM:249000)
Meckel syndrome, type 11 (OMIM:615397)
Meckel syndrome, type 2 (OMIM:603194)
Meckel syndrome, type 3 (OMIM:607361)
Meckel syndrome, type 8 (OMIM:613885)
Megalencephaly-capillary malformation-polymicrogyria syndrome (Orphanet:60040)
Miller-Dieker syndrome (Orphanet:531)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)
Nephronophthisis 15 (OMIM:614845)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Orofaciodigital syndrome type 8 (Orphanet:2755)
Orofaciodigital syndrome type 9 (Orphanet:141007)
Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)
Senior-Loken syndrome 8 (OMIM:616307)
Senior-Loken syndrome 9 (OMIM:616629)
Septo-optic dysplasia (Orphanet:3157)
Short-rib thoracic dysplasia 1 with or without polydactyly (OMIM:208500)
Short-rib thoracic dysplasia 7 with or without polydactyly (OMIM:614091)
Syndactyly type 4 (Orphanet:93405)
Synpolydactyly type 2 (Orphanet:295197)
Terminal transverse defects of arm (Orphanet:93937)
Wolf-Hirschhorn syndrome (Orphanet:280)