Preaxial polydactyly
Symptom Information:
Symptom ID: | HPO:0100258 | ||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |