Postaxial polydactyly
Symptom Information:
Symptom ID: | HPO:0100259 | |||||||||
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) Postaxial polydactyly(HPO:0100259) MedDRA: |
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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) |