Polydactyly
Symptom Information:
Symptom ID: | HPO:0010442 | |||||||||
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) MedDRA: |
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Database Frequency: | 69 / 7739 | |||||||||
Resource: |
All diseases associated with this symptom:
3C syndrome | (Orphanet:7) |
Absent tibia - polydactyly | (Orphanet:988) |
Acro-renal-mandibular syndrome | (Orphanet:958) |
Acrocephalopolydactyly | (Orphanet:221054) |
Bardet-Biedl syndrome | (Orphanet:110) |
Bardet-Biedl syndrome 1 | (OMIM:209900 ) |
Bardet-Biedl syndrome 10 | (OMIM:615987) |
Bardet-Biedl syndrome 11 | (OMIM:615988) |
Bardet-Biedl syndrome 12 | (OMIM:615989) |
Bardet-Biedl syndrome 13 | (OMIM:615990) |
Bardet-Biedl syndrome 19 | (OMIM:615996) |
Bardet-Biedl syndrome 2 | (OMIM:615981) |
Bardet-Biedl syndrome 3 | (OMIM:600151) |
Bardet-Biedl syndrome 4 | (OMIM:615982) |
Bardet-Biedl syndrome 5 | (OMIM:615983) |
Bardet-Biedl syndrome 6 | (OMIM:605231) |
Bardet-Biedl syndrome 7 | (OMIM:615984) |
Bardet-Biedl syndrome 8 | (OMIM:615985) |
Bardet-Biedl syndrome 9 | (OMIM:615986) |
Beckwith-Wiedemann syndrome due to CDKN1C mutation | (Orphanet:231120) |
Bloom syndrome | (Orphanet:125) |
Brachydactyly type C | (Orphanet:93384) |
Branchio-oculo-facial syndrome | (Orphanet:1297) |
Camptobrachydactyly | (Orphanet:1319) |
Constriction rings syndrome | (Orphanet:295000) |
Diabetic embryopathy | (Orphanet:1926) |
Ectrodactyly - polydactyly | (Orphanet:1892) |
FACIOCARDIOMELIC SYNDROME | (OMIM:612731) |
Focal dermal hypoplasia | (Orphanet:2092) |
Goodman syndrome | (Orphanet:65798) |
Gorlin syndrome | (Orphanet:377) |
Greenberg dysplasia | (Orphanet:1426) |
Hirschsprung disease - deafness - polydactyly | (Orphanet:2155) |
Holzgreve-Wagner-Rehder syndrome | (Orphanet:2167) |
Hypertelorism - hypospadias - polysyndactyly syndrome | (Orphanet:2211) |
Hypoplastic tibiae - postaxial polydactyly | (Orphanet:3332) |
Ito hypomelanosis | (Orphanet:435) |
Joubert syndrome 15 | (OMIM:614464) |
Joubert syndrome 16 | (OMIM:614465) |
Joubert syndrome 17 | (OMIM:614615) |
Joubert syndrome 18 | (OMIM:614815) |
Joubert syndrome 2 | (OMIM:608091) |
Joubert syndrome 22 | (OMIM:615665) |
Joubert syndrome 28 | (OMIM:617121) |
Klippel-Trénaunay syndrome | (Orphanet:90308) |
Meckel syndrome, type 1 | (OMIM:249000) |
Meckel syndrome, type 11 | (OMIM:615397) |
Meckel syndrome, type 2 | (OMIM:603194) |
Meckel syndrome, type 3 | (OMIM:607361) |
Meckel syndrome, type 8 | (OMIM:613885) |
Megalencephaly-capillary malformation-polymicrogyria syndrome | (Orphanet:60040) |
Miller-Dieker syndrome | (Orphanet:531) |
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency | (Orphanet:1194) |
Nephronophthisis 15 | (OMIM:614845) |
Orofaciodigital syndrome type 1 | (Orphanet:2750) |
Orofaciodigital syndrome type 8 | (Orphanet:2755) |
Orofaciodigital syndrome type 9 | (Orphanet:141007) |
PELGER-HUET ANOMALY | (OMIM:169400) |
Rubinstein-Taybi syndrome due to CREBBP mutations | (Orphanet:353277) |
Senior-Loken syndrome 8 | (OMIM:616307) |
Senior-Loken syndrome 9 | (OMIM:616629) |
Septo-optic dysplasia | (Orphanet:3157) |
Short-rib thoracic dysplasia 1 with or without polydactyly | (OMIM:208500) |
Short-rib thoracic dysplasia 7 with or without polydactyly | (OMIM:614091) |
Syndactyly type 4 | (Orphanet:93405) |
Synpolydactyly type 2 | (Orphanet:295197) |
TRIPHALANGEAL THUMB, NONOPPOSABLE | (OMIM:190600) |
Terminal transverse defects of arm | (Orphanet:93937) |
Wolf-Hirschhorn syndrome | (Orphanet:280) |