Preaxial polydactyly

Symptom Information:

Symptom ID: HPO:0100258
Synonyms:
Preaxial polydactyly [OMIM:Preaxial polydactyly]
Polydactyly, preaxial (rare) [OMIM:Polydactyly, preaxial (rare)]
Preaxial polydactyly (rare) [OMIM:Preaxial polydactyly (rare)]
Preaxial polydactyly (variable) [OMIM:Preaxial polydactyly (variable)]
Quality:
Cross references:
OMIM: "Preaxial polydactyly" [OMIM:Preaxial 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)]
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)
                         Preaxial polydactyly(HPO:0100258)
MedDRA:
Database Frequency: 39 / 7739
Resource:

All diseases associated with this symptom:

Acro-pectoral syndrome (Orphanet:85203)
Acro-renal-ocular syndrome (Orphanet:959)
Acromelic frontonasal dysplasia (Orphanet:1827)
Apert syndrome (Orphanet:87)
Biemond syndrome type 2 (Orphanet:141333)
Braddock syndrome (Orphanet:52047)
CARPENTER SYNDROME 1 (OMIM:201000)
CARPENTER SYNDROME 2 (OMIM:614976)
CERVICAL RIBS, SPRENGEL ANOMALY, ANAL ATRESIA, AND URETHRAL OBSTRUCTION (OMIM:601389)
Curry-Jones syndrome (Orphanet:1553)
ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE ANDPREAXIAL POLYDACTYLY OF FEET (OMIM:129540)
Femoral-facial syndrome (Orphanet:1988)
Greig cephalopolysyndactyly syndrome (Orphanet:380)
HYDROLETHALUS SYNDROME 1 (OMIM:236680)
HYDROLETHALUS SYNDROME 2 (OMIM:614120)
Lacrimo-auriculo-dento-digital syndrome (Orphanet:2363)
MICROCEPHALY, CORPUS CALLOSUM DYSGENESIS, AND CLEFT LIP/PALATE (OMIM:601420)
Mandibulofacial dysostosis-microcephaly syndrome (Orphanet:79113)
Microphthalmia with brain and digit anomalies (Orphanet:139471)
OROFACIODIGITAL SYNDROME VI (OMIM:277170)
Okihiro syndrome (Orphanet:93293)
Orofaciodigital syndrome type 10 (Orphanet:2756)
Orofaciodigital syndrome type 2 (Orphanet:2751)
Polydactyly of a biphalangeal thumb (Orphanet:93339)
Polydactyly of a triphalangeal thumb (Orphanet:93336)
Polydactyly of an index finger (Orphanet:93337)
Polysyndactyly (Orphanet:93338)
Polysyndactyly - cardiac malformation (Orphanet:2934)
Postaxial polydactyly type A (Orphanet:93334)
SANTOS SYNDROME (OMIM:613005)
Sakati-Nyhan syndrome (Orphanet:3128)
Short-rib thoracic dysplasia 13 with or without polydactyly (OMIM:616300)
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 8 with or without polydactyly (OMIM:615503)
Synpolydactyly type 1 (Orphanet:295195)
Townes-Brocks syndrome (Orphanet:857)
Triphalangeal thumb - polysyndactyly syndrome (Orphanet:2950)
VACTERL/VATER association (Orphanet:887)