Syndactyly
Symptom Information:
Symptom ID: | HPO:0001159 | ||||||||||||||||||||||
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) Syndactyly(HPO:0001159) MedDRA: |
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Database Frequency: | 140 / 7739 | ||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
3C syndrome | (Orphanet:7) |
8q21.11 microdeletion syndrome | (Orphanet:284160) |
AARSKOG-SCOTT SYNDROME | (OMIM:305400) |
ADAMS-OLIVER SYNDROME 1 | (OMIM:100300) |
ADAMS-OLIVER SYNDROME 5 | (OMIM:616028) |
ADULT syndrome | (Orphanet:978) |
AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM | (OMIM:104350) |
ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib | (OMIM:615631) |
Aarskog-Scott syndrome | (Orphanet:915) |
Acro-renal-mandibular syndrome | (Orphanet:958) |
Acro-renal-ocular syndrome | (Orphanet:959) |
Acromelic frontonasal dysplasia | (Orphanet:1827) |
Angio-osteohypertrophic syndrome | (Orphanet:2346) |
Autosomal recessive facio-digito-genital syndrome | (Orphanet:1974) |
Autosomal recessive multiple pterygium syndrome | (Orphanet:2990) |
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA | (OMIM:609945) |
Bardet-Biedl syndrome | (Orphanet:110) |
Bardet-Biedl syndrome 1 | (OMIM:209900 ) |
Bardet-Biedl syndrome 10 | (OMIM:615987) |
Bardet-Biedl syndrome 12 | (OMIM:615989) |
Bardet-Biedl syndrome 2 | (OMIM:615981) |
Bardet-Biedl syndrome 4 | (OMIM:615982) |
Bardet-Biedl syndrome 6 | (OMIM:605231) |
Bardet-Biedl syndrome 7 | (OMIM:615984) |
Bardet-Biedl syndrome 9 | (OMIM:615986) |
Bartsocas-Papas syndrome | (Orphanet:1234) |
Bloom syndrome | (Orphanet:125) |
Bohring-Opitz syndrome | (Orphanet:97297) |
Brachydactyly type A2 | (Orphanet:93396) |
Brachydactyly type B | (Orphanet:93383) |
C syndrome | (Orphanet:1308) |
CARPENTER SYNDROME 1 | (OMIM:201000) |
CORNELIA DE LANGE SYNDROME 4 | (OMIM:614701) |
Camptobrachydactyly | (Orphanet:1319) |
Camptodactyly syndrome, Guadalajara type 1 | (Orphanet:1327) |
Cardiodysrhythmic potassium-sensitive periodic paralysis | (Orphanet:37553) |
Cenani-Lenz syndrome | (Orphanet:3258) |
Charcot-Marie-Tooth disease type 4B3 | (Orphanet:363981) |
Congenital dyserythropoietic anemia type I | (Orphanet:98869) |
Constriction rings syndrome | (Orphanet:295000) |
Cranioectodermal dysplasia 2 | (OMIM:613610) |
Cranioectodermal dysplasia 3 | (OMIM:614099) |
Craniofacial dysplasia-osteopenia syndrome | (Orphanet:314555) |
Craniofrontonasal dysplasia | (Orphanet:1520) |
Craniosynostosis and dental anomalies | (Orphanet:284149) |
Curry-Jones syndrome | (Orphanet:1553) |
Diaphragmatic defect - limb deficiency - skull defect | (Orphanet:2141) |
Distal monosomy 10q | (Orphanet:96148) |
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1 | (OMIM:129900) |
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 | (OMIM:604292) |
EEM syndrome | (Orphanet:1897) |
Endocrine-cerebro-osteodysplasia syndrome | (Orphanet:199332) |
FIBULAR APLASIA, TIBIAL CAMPOMELIA, AND OLIGOSYNDACTYLY SYNDROME | (OMIM:246570) |
Faciocardiorenal syndrome | (Orphanet:1973) |
Fibulo-ulnar hypoplasia - renal anomalies | (Orphanet:2256) |
Focal dermal hypoplasia | (Orphanet:2092) |
Fraser syndrome | (Orphanet:2052) |
Fuhrmann syndrome | (Orphanet:2854) |
Goodman syndrome | (Orphanet:65798) |
Greig cephalopolysyndactyly syndrome | (Orphanet:380) |
Hallux varus - preaxial polysyndactyly | (Orphanet:2110) |
Hartsfield-Bixler-Demyer syndrome | (Orphanet:2117) |
Heart-hand syndrome, Slovenian type | (Orphanet:168796) |
Hypertelorism - hypospadias - polysyndactyly syndrome | (Orphanet:2211) |
Hypoplastic tibiae - postaxial polydactyly | (Orphanet:3332) |
Ito hypomelanosis | (Orphanet:435) |
Jawad syndrome | (Orphanet:313795) |
Joubert syndrome 17 | (OMIM:614615) |
Joubert syndrome 20 | (OMIM:614970) |
Joubert syndrome 22 | (OMIM:615665) |
KBG syndrome | (Orphanet:2332) |
Klippel-Trénaunay syndrome | (Orphanet:90308) |
LOEYS-DIETZ SYNDROME 2 | (OMIM:610168) |
Langer-Giedion syndrome | (Orphanet:502) |
Lathosterolosis | (Orphanet:46059) |
Laurin-Sandrow syndrome | (Orphanet:2378) |
Lenz-Majewski hyperostotic dwarfism | (Orphanet:2658) |
Limb-mammary syndrome | (Orphanet:69085) |
MICROPHTHALMIA, SYNDROMIC 1 | (OMIM:309800) |
McKusick-Kaufman syndrome | (Orphanet:2473) |
Meckel syndrome | (Orphanet:564) |
Meckel syndrome, type 1 | (OMIM:249000) |
Megalencephaly-capillary malformation-polymicrogyria syndrome | (Orphanet:60040) |
Microduplication Xp11.22-p11.23 syndrome | (Orphanet:217377) |
Microphthalmia with brain and digit anomalies | (Orphanet:139471) |
Microphthalmia with limb anomalies | (Orphanet:1106) |
Moebius syndrome | (Orphanet:570) |
Monosomy 18q | (Orphanet:1600) |
Monosomy 5p | (Orphanet:281) |
Nager syndrome | (Orphanet:245) |
OPITZ-KAVEGGIA SYNDROME | (OMIM:305450) |
OROFACIODIGITAL SYNDROME VI | (OMIM:277170) |
Okihiro syndrome | (Orphanet:93293) |
Orofaciodigital syndrome type 1 | (Orphanet:2750) |
Orofaciodigital syndrome type 2 | (Orphanet:2751) |
Orofaciodigital syndrome type 4 | (Orphanet:2753) |
Orofaciodigital syndrome type 8 | (Orphanet:2755) |
Orofaciodigital syndrome type 9 | (Orphanet:141007) |
Otopalatodigital syndrome type 2 | (Orphanet:90652) |
Pallister-Hall syndrome | (Orphanet:672) |
Pelviscapular dysplasia | (Orphanet:93333) |
Peters-plus syndrome | (Orphanet:709) |
Poland syndrome | (Orphanet:2911) |
Polysyndactyly - cardiac malformation | (Orphanet:2934) |
Postaxial acrofacial dysostosis | (Orphanet:246) |
Postaxial polydactyly - dental and vertebral anomalies | (Orphanet:2916) |
Postaxial polydactyly type A | (Orphanet:93334) |
Prader-Willi syndrome | (Orphanet:739) |
Pseudoaminopterin syndrome | (Orphanet:221120) |
RAPP-HODGKIN SYNDROME | (OMIM:129400) |
ROBERTS SYNDROME | (OMIM:268300) |
Radio-ulnar synostosis - amegakaryocytic thrombocytopenia | (Orphanet:71289) |
Roberts syndrome | (Orphanet:3103) |
Rubinstein-Taybi syndrome due to CREBBP mutations | (Orphanet:353277) |
SANTOS SYNDROME | (OMIM:613005) |
SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY | (OMIM:614800) |
SPINAL MUSCULAR ATROPHY WITH MENTAL RETARDATION | (OMIM:271109) |
SPLIT-HAND/FOOT MALFORMATION 4 | (OMIM:605289) |
Saethre-Chotzen syndrome | (Orphanet:794) |
Sakati-Nyhan syndrome | (Orphanet:3128) |
Schilbach-Rott syndrome | (Orphanet:2353) |
Short-rib thoracic dysplasia 7 with or without polydactyly | (OMIM:614091) |
Short-rib thoracic dysplasia 8 with or without polydactyly | (OMIM:615503) |
Silver-Russell syndrome | (Orphanet:813) |
Split hand-split foot malformation | (Orphanet:2440) |
Stapes ankylosis with broad thumbs and toes | (Orphanet:140917) |
Summitt syndrome | (Orphanet:3210) |
Symphalangism with multiple anomalies of hands and feet | (Orphanet:3246) |
Syndactyly - camptodactyly and clinodactyly of fifth fingers - bifid toes | (Orphanet:357332) |
Syndactyly type 3 | (Orphanet:93404) |
Synpolydactyly type 2 | (Orphanet:295197) |
TUKEL SYNDROME | (OMIM:609428) |
Temtamy preaxial brachydactyly syndrome | (Orphanet:363417) |
Timothy syndrome | (Orphanet:65283) |
Triphalangeal thumb - polysyndactyly syndrome | (Orphanet:2950) |
Ulnar/fibula ray defect - brachydactyly | (Orphanet:52056) |
VACTERL/VATER association | (Orphanet:887) |
Verloove Vanhorick-Brubakk syndrome | (Orphanet:3429) |
Waardenburg syndrome type 3 | (Orphanet:896) |
Yunis-Varon syndrome | (Orphanet:3472) |