Hand polydactyly
Symptom Information:
Symptom ID: | HPO:0001161 | ||||||||||||||||||
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) Hand polydactyly(HPO:0001161) Abnormality of finger(HPO:0001167) Abnormality of phalanx of finger(HPO:0005918) Duplication of phalanx of hand(HPO:0009997) Hand polydactyly(HPO:0001161) Abnormality of the upper limb(HPO:0002817) 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) Abnormality of the hand(HPO:0001155) Duplication of hand bones(HPO:0004275) Duplication of phalanx of hand(HPO:0009997) Hand polydactyly(HPO:0001161) Abnormality of finger(HPO:0001167) Abnormality of phalanx of finger(HPO:0005918) Duplication of phalanx of hand(HPO:0009997) Hand polydactyly(HPO:0001161) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Musculoskeletal and connective tissue disorders congenital(MedDRA:10028396) Musculoskeletal and connective tissue disorders of limbs congenital(MedDRA:10028381) Hand polydactyly(HPO:0001161) |
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Database Frequency: | 71 / 7739 | ||||||||||||||||||
Resource: |
All diseases associated with this symptom:
16p13.11 microduplication syndrome | (Orphanet:261243) |
1p36 deletion syndrome | (Orphanet:1606) |
1q21.1 microdeletion syndrome | (Orphanet:250989) |
22q11.2 deletion syndrome | (Orphanet:567) |
3C syndrome | (Orphanet:7) |
Absent tibia - polydactyly | (Orphanet:988) |
Acro-pectoro-renal dysplasia | (Orphanet:956) |
Acro-renal-mandibular syndrome | (Orphanet:958) |
Acrocephalopolydactyly | (Orphanet:221054) |
Angio-osteohypertrophic syndrome | (Orphanet:2346) |
Antecubital pterygium syndrome | (Orphanet:2987) |
Bardet-Biedl syndrome | (Orphanet:110) |
Bardet-Biedl syndrome 12 | (OMIM:615989) |
Bardet-Biedl syndrome 2 | (OMIM:615981) |
Bardet-Biedl syndrome 4 | (OMIM:615982) |
Bardet-Biedl syndrome 7 | (OMIM:615984) |
Bardet-Biedl syndrome 9 | (OMIM:615986) |
Bloom syndrome | (Orphanet:125) |
C syndrome | (Orphanet:1308) |
CHARGE syndrome | (Orphanet:138) |
Camptobrachydactyly | (Orphanet:1319) |
Char syndrome | (Orphanet:46627) |
Constriction rings syndrome | (Orphanet:295000) |
Craniofrontonasal dysplasia | (Orphanet:1520) |
DISORGANIZATION, MOUSE, HOMOLOG OF | (OMIM:223200) |
Diabetic embryopathy | (Orphanet:1926) |
EEC syndrome | (Orphanet:1896) |
Ectodermal dysplasia syndrome | (Orphanet:79373) |
Ellis Van Creveld syndrome | (Orphanet:289) |
Focal dermal hypoplasia | (Orphanet:2092) |
Goodman syndrome | (Orphanet:65798) |
Gorlin syndrome | (Orphanet:377) |
Harlequin ichthyosis | (Orphanet:457) |
Heart-hand syndrome type 2 | (Orphanet:1350) |
Hidrotic ectodermal dysplasia | (Orphanet:189) |
Hirschsprung disease - deafness - polydactyly | (Orphanet:2155) |
Holoprosencephaly | (Orphanet:2162) |
Holzgreve-Wagner-Rehder syndrome | (Orphanet:2167) |
Hypertelorism - hypospadias - polysyndactyly syndrome | (Orphanet:2211) |
Ito hypomelanosis | (Orphanet:435) |
Jacobsen syndrome | (Orphanet:2308) |
Jeune syndrome | (Orphanet:474) |
Joubert syndrome | (Orphanet:475) |
Joubert syndrome 15 | (OMIM:614464) |
Joubert syndrome 16 | (OMIM:614465) |
Joubert syndrome 17 | (OMIM:614615) |
Joubert syndrome with ocular defect | (Orphanet:220493) |
Joubert syndrome with oculorenal defect | (Orphanet:2318) |
Joubert syndrome with orofaciodigital defect | (Orphanet:2754) |
Joubert syndrome with renal defect | (Orphanet:220497) |
Laurence-Moon syndrome | (Orphanet:2377) |
Laurin-Sandrow syndrome | (Orphanet:2378) |
MESOAXIAL HEXADACTYLY AND CARDIAC MALFORMATION | (OMIM:249670) |
Megalencephaly-capillary malformation-polymicrogyria syndrome | (Orphanet:60040) |
Microphthalmia with limb anomalies | (Orphanet:1106) |
Nephronophthisis 15 | (OMIM:614845) |
Neuroectodermal syndrome, Johnson type | (Orphanet:2316) |
Oculocerebrocutaneous syndrome | (Orphanet:1647) |
Oculodentodigital dysplasia | (Orphanet:2710) |
Orofaciodigital syndrome type 1 | (Orphanet:2750) |
Orofaciodigital syndrome type 9 | (Orphanet:141007) |
Otopalatodigital syndrome | (Orphanet:669) |
PELGER-HUET ANOMALY | (OMIM:169400) |
Peroxisomal acyl-CoA oxidase deficiency | (Orphanet:2971) |
Proximal 16p11.2 microdeletion syndrome | (Orphanet:261197) |
SHORT syndrome | (Orphanet:3163) |
Schinzel-Giedion syndrome | (Orphanet:798) |
Smith-Magenis syndrome | (Orphanet:819) |
Syndactyly type 4 | (Orphanet:93405) |
Syndrome with brachydactyly | (Orphanet:69028) |
VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS | (OMIM:314390) |