Postaxial hand polydactyly
Symptom Information:
Symptom ID: | HPO:0001162 | |||||||||||||||||
Synonyms: |
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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) Postaxial hand polydactyly(HPO:0001162) Hand polydactyly(HPO:0001161) Postaxial hand polydactyly(HPO:0001162) Abnormality of finger(HPO:0001167) Abnormality of the 5th finger(HPO:0004207) Postaxial hand polydactyly(HPO:0001162) Abnormality of phalanx of finger(HPO:0005918) Duplication of phalanx of hand(HPO:0009997) Hand polydactyly(HPO:0001161) Postaxial hand polydactyly(HPO:0001162) Abnormality of the upper limb(HPO:0002817) Abnormality of the hand(HPO:0001155) Duplication of hand bones(HPO:0004275) Duplication of phalanx of hand(HPO:0009997) Hand polydactyly(HPO:0001161) Postaxial hand polydactyly(HPO:0001162) Abnormality of finger(HPO:0001167) Abnormality of the 5th finger(HPO:0004207) Postaxial hand polydactyly(HPO:0001162) Abnormality of phalanx of finger(HPO:0005918) Duplication of phalanx of hand(HPO:0009997) Hand polydactyly(HPO:0001161) Postaxial hand polydactyly(HPO:0001162) Duplication of bones involving the upper extremities(HPO:0009142) Duplication of hand bones(HPO:0004275) Duplication of phalanx of hand(HPO:0009997) Hand polydactyly(HPO:0001161) Postaxial hand polydactyly(HPO:0001162) MedDRA: |
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Database Frequency: | 119 / 7739 | |||||||||||||||||
Resource: |
All diseases associated with this symptom:
Absent tibia - polydactyly - arachnoid cyst | (Orphanet:3328) |
Acalvaria | (Orphanet:945) |
Achondrogenesis type 2 | (Orphanet:93296) |
Acrocallosal syndrome | (Orphanet:36) |
Acrocephalopolydactyly | (Orphanet:221054) |
Acrofacial dysostosis, Weyers type | (Orphanet:952) |
Acromesomelic dysplasia, Grebe type | (Orphanet:2098) |
Apert syndrome | (Orphanet:87) |
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA | (OMIM:609945) |
BRESEK syndrome | (Orphanet:85284) |
Bardet-Biedl syndrome | (Orphanet:110) |
Bardet-Biedl syndrome 10 | (OMIM:615987) |
Bardet-Biedl syndrome 17 | (OMIM:615994) |
Bardet-Biedl syndrome 3 | (OMIM:600151) |
Bardet-Biedl syndrome 4 | (OMIM:615982) |
Beckwith-Wiedemann syndrome due to 11p15 microduplication | (Orphanet:96076) |
Brachydactyly - nystagmus - cerebellar ataxia | (Orphanet:1246) |
Brain malformation - congenital heart disease - postaxial polydactyly | (Orphanet:75389) |
C syndrome | (Orphanet:1308) |
CARPENTER SYNDROME 2 | (OMIM:614976) |
CONE-ROD DYSTROPHY 16 | (OMIM:614500) |
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl | (OMIM:614576) |
Carpenter syndrome | (Orphanet:65759) |
Cerebro-facio-thoracic dysplasia | (Orphanet:1394) |
Cerebro-oculo-nasal syndrome | (Orphanet:66625) |
Cortical blindness - intellectual deficit - polydactyly | (Orphanet:1389) |
Crossed polysyndactyly | (Orphanet:2935) |
Dandy-Walker malformation - postaxial polydactyly | (Orphanet:1566) |
Distal monosomy 3p | (Orphanet:1620) |
EVC2 GENE | (OMIM:607261) |
Ectrodactyly - polydactyly | (Orphanet:1892) |
Ellis Van Creveld syndrome | (Orphanet:289) |
Focal dermal hypoplasia | (Orphanet:2092) |
Frontonasal dysplasia | (Orphanet:250) |
Fuhrmann syndrome | (Orphanet:2854) |
Genito-palato-cardiac syndrome | (Orphanet:2075) |
Greenberg dysplasia | (Orphanet:1426) |
Greig cephalopolysyndactyly syndrome | (Orphanet:380) |
Guttmacher syndrome | (Orphanet:2957) |
HOLOPROSENCEPHALY 9 | (OMIM:610829) |
HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED | (OMIM:241800) |
Hand-foot-genital syndrome | (Orphanet:2438) |
Heart defect - tongue hamartoma - polysyndactyly | (Orphanet:1338) |
Hirschsprung disease - deafness - polydactyly | (Orphanet:2155) |
Holoprosencephaly - postaxial polydactyly | (Orphanet:2166) |
Hydrolethalus | (Orphanet:2189) |
Hypoplastic tibiae - postaxial polydactyly | (Orphanet:3332) |
Ichthyosis follicularis - alopecia - photophobia | (Orphanet:2273) |
Intellectual deficit - polydactyly - uncombable hair | (Orphanet:3082) |
Jeune syndrome | (Orphanet:474) |
Joubert syndrome | (Orphanet:475) |
Joubert syndrome 1 | (OMIM:213300) |
Joubert syndrome 2 | (OMIM:608091) |
Joubert syndrome 20 | (OMIM:614970) |
Joubert syndrome 22 | (OMIM:615665) |
Joubert syndrome with hepatic defect | (Orphanet:1454) |
Joubert syndrome with oculorenal defect | (Orphanet:2318) |
KBG syndrome | (Orphanet:2332) |
LOEYS-DIETZ SYNDROME 1 | (OMIM:609192) |
LOEYS-DIETZ SYNDROME 2 | (OMIM:610168) |
Lathosterolosis | (Orphanet:46059) |
Lethal Larsen-like syndrome | (Orphanet:2371) |
Loeys-Dietz syndrome type 1 | (Orphanet:60030) |
MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 2 | (OMIM:615937) |
MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 3 | (OMIM:615938) |
McKusick-Kaufman syndrome | (Orphanet:2473) |
Meckel syndrome | (Orphanet:564) |
Meckel syndrome, type 2 | (OMIM:603194) |
Meckel syndrome, type 3 | (OMIM:607361) |
Meckel syndrome, type 4 | (OMIM:611134) |
Meckel syndrome, type 5 | (OMIM:611561) |
Meckel syndrome, type 6 | (OMIM:612284) |
Meckel syndrome, type 8 | (OMIM:613885) |
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus | (Orphanet:83473) |
Microcephaly - seizures - intellectual deficit - heart disease | (Orphanet:2519) |
Microphthalmia with limb anomalies | (Orphanet:1106) |
Monosomy 9p | (Orphanet:261112) |
Mullerian derivatives - lymphangiectasia - polydactyly | (Orphanet:1655) |
Mullerian duct anomalies - limb anomalies | (Orphanet:2491) |
Multinodular goiter - cystic kidney - polydactyly | (Orphanet:2091) |
Non-distal trisomy 13q | (Orphanet:1702) |
Non-rhizomelic chondrodysplasia punctata | (Orphanet:176) |
Oliver syndrome | (Orphanet:2920) |
Orofaciodigital syndrome type 1 | (Orphanet:2750) |
Orofaciodigital syndrome type 2 | (Orphanet:2751) |
Orofaciodigital syndrome type 3 | (Orphanet:2752) |
Orofaciodigital syndrome type 4 | (Orphanet:2753) |
Orofaciodigital syndrome type 5 | (Orphanet:2919) |
Orofaciodigital syndrome type 8 | (Orphanet:2755) |
Otopalatodigital syndrome | (Orphanet:669) |
POLYDACTYLY, POSTAXIAL, TYPE A2 | (OMIM:602085) |
POLYDACTYLY, POSTAXIAL, TYPE A5 | (OMIM:263450) |
POLYDACTYLY, POSTAXIAL, TYPE A6 | (OMIM:615226) |
Pallister-Hall syndrome | (Orphanet:672) |
Polydactyly-myopia syndrome | (Orphanet:2917) |
Polysyndactyly - cardiac malformation | (Orphanet:2934) |
Postaxial polydactyly - dental and vertebral anomalies | (Orphanet:2916) |
Postaxial polydactyly type A | (Orphanet:93334) |
Postaxial tetramelic oligodactyly | (Orphanet:2730) |
Scalp defects - postaxial polydactyly | (Orphanet:1003) |
Schinzel-Giedion syndrome | (Orphanet:798) |
Short rib-polydactyly syndrome | (Orphanet:1505) |
Short rib-polydactyly syndrome, Majewski type | (Orphanet:93269) |
Short rib-polydactyly syndrome, Verma-Naumoff type | (Orphanet:93271) |
Short-rib thoracic dysplasia 10 with or without polydactyly | (OMIM:615630) |
Short-rib thoracic dysplasia 2 with or without polydactyly | (OMIM:611263) |
Simpson-Golabi-Behmel syndrome | (Orphanet:373) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
Syndactyly type 2 | (Orphanet:93403) |
Syndactyly-polydactyly-ear lobe syndrome | (Orphanet:3259) |
THAI SYMPHALANGISM SYNDROME | (OMIM:608028) |
Tetrasomy 12p | (Orphanet:884) |
Tibial aplasia - ectrodactyly | (Orphanet:3329) |
Triphalangeal thumb - polysyndactyly syndrome | (Orphanet:2950) |
Trisomy 13 | (Orphanet:3378) |
Trisomy 18 | (Orphanet:3380) |
Ulnar-mammary syndrome | (Orphanet:3138) |
VENTRICULOMEGALY WITH CYSTIC KIDNEY DISEASE | (OMIM:219730) |
X-linked dominant chondrodysplasia punctata | (Orphanet:35173) |