Finger syndactyly
Symptom Information:
Symptom ID: | HPO:0006101 | |||
Synonyms: |
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Quality: | ||||
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) Finger syndactyly(HPO:0006101) MedDRA: |
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Database Frequency: | 198 / 7739 | |||
Resource: |
All diseases associated with this symptom:
14q22q23 microdeletion syndrome | (Orphanet:264200) |
15q11q13 microduplication syndrome | (Orphanet:238446) |
15q24 microdeletion syndrome | (Orphanet:94065) |
17q12 microduplication syndrome | (Orphanet:261272) |
19p13.12 microdeletion syndrome | (Orphanet:254346) |
19q13.11 microdeletion syndrome | (Orphanet:217346) |
2q31.1 microdeletion syndrome | (Orphanet:251014) |
2q37 microdeletion syndrome | (Orphanet:1001) |
3C syndrome | (Orphanet:7) |
6p22 microdeletion syndrome | (Orphanet:251046) |
8q21.11 microdeletion syndrome | (Orphanet:284160) |
8q22.1 microdeletion syndrome | (Orphanet:178303) |
ADULT syndrome | (Orphanet:978) |
Aarskog-Scott syndrome | (Orphanet:915) |
Ackerman syndrome | (Orphanet:2561) |
Acro-cardio-facial syndrome | (Orphanet:2008) |
Acro-oto-ocular syndrome | (Orphanet:2980) |
Acro-pectoral syndrome | (Orphanet:85203) |
Acro-pectoro-renal dysplasia | (Orphanet:956) |
Acro-renal-mandibular syndrome | (Orphanet:958) |
Acro-renal-ocular syndrome | (Orphanet:959) |
Acrocallosal syndrome | (Orphanet:36) |
Acrofacial dysostosis, Catania type | (Orphanet:1786) |
Acrofacial dysostosis, Palagonia type | (Orphanet:1787) |
Acrofacial dysostosis, Rodriguez type | (Orphanet:1788) |
Acropectorovertebral dysplasia | (Orphanet:957) |
Adams-Oliver syndrome | (Orphanet:974) |
Alopecia - contractures - dwarfism - intellectual deficit | (Orphanet:1005) |
Aminopterin/methotrexate embryofetopathy | (Orphanet:1908) |
Amniotic bands | (Orphanet:1034) |
Angio-osteohypertrophic syndrome | (Orphanet:2346) |
Ankyloblepharon - ectodermal defects - cleft lip/palate | (Orphanet:1071) |
Apert syndrome | (Orphanet:87) |
Aphalangy - hemivertebrae - urogenital-intestinal dysgenesis | (Orphanet:1112) |
Autosomal dominant Larsen syndrome | (Orphanet:503) |
Autosomal dominant Robinow syndrome | (Orphanet:3107) |
Autosomal dominant popliteal pterygium syndrome | (Orphanet:1300) |
Autosomal recessive Robinow syndrome | (Orphanet:1507) |
Autosomal recessive facio-digito-genital syndrome | (Orphanet:1974) |
Autosomal recessive multiple pterygium syndrome | (Orphanet:2990) |
Autosomal recessive spondylocostal dysostosis | (Orphanet:2311) |
Bardet-Biedl syndrome | (Orphanet:110) |
Bardet-Biedl syndrome 4 | (OMIM:615982) |
Bartsocas-Papas syndrome | (Orphanet:1234) |
Blepharo-cheilo-odontic syndrome | (Orphanet:1997) |
Blepharonasofacial malformation syndrome | (Orphanet:1252) |
Bloom syndrome | (Orphanet:125) |
Boomerang dysplasia | (Orphanet:1263) |
Brachydactyly type B | (Orphanet:93383) |
Brachydactyly type B2 | (Orphanet:140908) |
Camptobrachydactyly | (Orphanet:1319) |
Camptodactyly - joint contractures - facial skeletal defects | (Orphanet:1323) |
Cenani-Lenz syndrome | (Orphanet:3258) |
Charlie M syndrome | (Orphanet:1406) |
Choroidal atrophy - alopecia | (Orphanet:1433) |
Cohen syndrome | (Orphanet:193) |
Crane-Heise syndrome | (Orphanet:1512) |
Cranioectodermal dysplasia | (Orphanet:1515) |
Craniofrontonasal dysplasia | (Orphanet:1520) |
Craniomicromelic syndrome | (Orphanet:1524) |
Craniosynostosis, Herrmann-Opitz type | (Orphanet:2145) |
Craniosynostosis, Philadelphia type | (Orphanet:1527) |
Crossed polysyndactyly | (Orphanet:2935) |
Curry-Jones syndrome | (Orphanet:1553) |
Cutis marmorata telangiectatica congenita | (Orphanet:1556) |
Deafness - genital anomalies - metacarpal and metatarsal synostosis | (Orphanet:3224) |
Diaphragmatic defect - limb deficiency - skull defect | (Orphanet:2141) |
Dystrophic epidermolysis bullosa | (Orphanet:303) |
EEC syndrome | (Orphanet:1896) |
EEM syndrome | (Orphanet:1897) |
Ectodermal dysplasia syndrome | (Orphanet:79373) |
Ectrodactyly - polydactyly | (Orphanet:1892) |
Embryonary disorganization syndrome | (Orphanet:1664) |
Epiphyseal dysplasia - hearing loss - dysmorphism | (Orphanet:1825) |
Eyebrow duplication - syndactyly | (Orphanet:3172) |
FACES syndrome | (Orphanet:1969) |
Fanconi anemia | (Orphanet:84) |
Femur-fibula-ulna complex | (Orphanet:2019) |
Fibulo-ulnar hypoplasia - renal anomalies | (Orphanet:2256) |
Filippi syndrome | (Orphanet:3255) |
Fine-Lubinsky syndrome | (Orphanet:1272) |
Focal dermal hypoplasia | (Orphanet:2092) |
Fraser syndrome | (Orphanet:2052) |
Fuhrmann syndrome | (Orphanet:2854) |
Goldberg-Shprintzen megacolon syndrome | (Orphanet:66629) |
Gordon syndrome | (Orphanet:376) |
Gorlin syndrome | (Orphanet:377) |
Grange syndrome | (Orphanet:79094) |
Greig cephalopolysyndactyly syndrome | (Orphanet:380) |
Heart defect - tongue hamartoma - polysyndactyly | (Orphanet:1338) |
Hennekam syndrome | (Orphanet:2136) |
Hereditary acrokeratotic poikiloderma, Weary type | (Orphanet:2907) |
Hereditary spastic paraplegia | (Orphanet:685) |
Hidrotic ectodermal dysplasia | (Orphanet:189) |
Holt-Oram syndrome | (Orphanet:392) |
Hypertelorism - hypospadias - polysyndactyly syndrome | (Orphanet:2211) |
Hypertelorism, Teebi type | (Orphanet:1519) |
Hypertrichotic osteochondrodysplasia, Cantu type | (Orphanet:1517) |
Hypoglossia - hypodactyly | (Orphanet:989) |
Hypoplastic tibiae - postaxial polydactyly | (Orphanet:3332) |
Incontinentia pigmenti | (Orphanet:464) |
Intellectual deficit - spasticity - ectrodactyly | (Orphanet:1891) |
Isolated cloverleaf skull syndrome | (Orphanet:2343) |
Jackson-Weiss syndrome | (Orphanet:1540) |
Jacobsen syndrome | (Orphanet:2308) |
Junctional epidermolysis bullosa | (Orphanet:305) |
Junctional epidermolysis bullosa, Herlitz type | (Orphanet:79404) |
KBG syndrome | (Orphanet:2332) |
Kindler syndrome | (Orphanet:2908) |
Lacrimo-auriculo-dento-digital syndrome | (Orphanet:2363) |
Laurence-Moon syndrome | (Orphanet:2377) |
Laurin-Sandrow syndrome | (Orphanet:2378) |
Lenz-Majewski hyperostotic dwarfism | (Orphanet:2658) |
Limb transversal defect - cardiac anomaly | (Orphanet:2492) |
Mal de Meleda | (Orphanet:87503) |
Malignant hyperthermia - arthrogryposis - torticollis | (Orphanet:2215) |
McKusick-Kaufman syndrome | (Orphanet:2473) |
Megalencephaly-capillary malformation-polymicrogyria syndrome | (Orphanet:60040) |
Mesoaxial synostotic syndactyly with phalangeal reduction | (Orphanet:157801) |
Mesomelic dwarfism, Nievergelt type | (Orphanet:2633) |
Microcephaly - intellectual deficit - phalangeal and neurological anomalies | (Orphanet:137658) |
Microphthalmia with brain and digit anomalies | (Orphanet:139471) |
Microphthalmia with limb anomalies | (Orphanet:1106) |
Microphthalmia, Lenz type | (Orphanet:568) |
Moebius syndrome | (Orphanet:570) |
Monosomy 13q14 | (Orphanet:1587) |
Monosomy 5p | (Orphanet:281) |
Mowat-Wilson syndrome | (Orphanet:2152) |
Multiple epiphyseal dysplasia, Al-Gazali type | (Orphanet:166024) |
Neu-Laxova syndrome | (Orphanet:2671) |
Nevus comedonicus syndrome | (Orphanet:64754) |
Oculocerebrocutaneous syndrome | (Orphanet:1647) |
Oculodentodigital dysplasia | (Orphanet:2710) |
Odontotrichomelic syndrome | (Orphanet:2723) |
Okamoto syndrome | (Orphanet:2729) |
Oliver syndrome | (Orphanet:2920) |
Orofaciodigital syndrome type 1 | (Orphanet:2750) |
Orofaciodigital syndrome type 2 | (Orphanet:2751) |
Orofaciodigital syndrome type 4 | (Orphanet:2753) |
Orofaciodigital syndrome type 5 | (Orphanet:2919) |
Orofaciodigital syndrome type 8 | (Orphanet:2755) |
Otopalatodigital syndrome | (Orphanet:669) |
Pallister-Hall syndrome | (Orphanet:672) |
Paraplegia - brachydactyly - cone-shaped epiphysis | (Orphanet:2823) |
Pfeiffer syndrome | (Orphanet:710) |
Pfeiffer syndrome type 1 | (Orphanet:93258) |
Pfeiffer syndrome type 2 | (Orphanet:93259) |
Pfeiffer syndrome type 3 | (Orphanet:93260) |
Poland syndrome | (Orphanet:2911) |
Polysyndactyly - cardiac malformation | (Orphanet:2934) |
Postaxial acrofacial dysostosis | (Orphanet:246) |
Proteus syndrome | (Orphanet:744) |
Proximal symphalangism | (Orphanet:3250) |
Radio-ulnar synostosis - amegakaryocytic thrombocytopenia | (Orphanet:71289) |
Recessive aplasia cutis congenita of limbs | (Orphanet:1115) |
Recessive dystrophic epidermolysis bullosa-generalized other | (Orphanet:89842) |
Roberts syndrome | (Orphanet:3103) |
Rubinstein-Taybi syndrome | (Orphanet:783) |
SPLIT-HAND/FOOT MALFORMATION 2 | (OMIM:313350) |
SPLIT-HAND/FOOT MALFORMATION 6 | (OMIM:225300) |
Saethre-Chotzen syndrome | (Orphanet:794) |
Schilbach-Rott syndrome | (Orphanet:2353) |
Sclerosteosis | (Orphanet:3152) |
Severe generalized recessive dystrophic epidermolysis bullosa | (Orphanet:79408) |
Short rib-polydactyly syndrome | (Orphanet:1505) |
Short stature - craniofacial anomalies - genital hypoplasia | (Orphanet:2994) |
Simpson-Golabi-Behmel syndrome | (Orphanet:373) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
Split hand - urinary anomalies - spina bifida | (Orphanet:2437) |
Split hand-split foot malformation | (Orphanet:2440) |
Summitt syndrome | (Orphanet:3210) |
Symphalangism with multiple anomalies of hands and feet | (Orphanet:3246) |
Syndactyly type 1 | (Orphanet:93402) |
Syndactyly type 2 | (Orphanet:93403) |
Syndactyly type 3 | (Orphanet:93404) |
Syndactyly type 4 | (Orphanet:93405) |
Syndactyly type 5 | (Orphanet:93406) |
Syndrome with brachydactyly | (Orphanet:69028) |
Synostosis - microcephaly - scoliosis | (Orphanet:3268) |
Synpolydactyly type 1 | (Orphanet:295195) |
Tel Hashomer camptodactyly syndrome | (Orphanet:3292) |
Thrombocytopenia - absent radius | (Orphanet:3320) |
Thumb deformity - alopecia - pigmentation anomaly | (Orphanet:2251) |
Tibial aplasia - ectrodactyly | (Orphanet:3329) |
Tricho-oculo-dermo-vertebral syndrome | (Orphanet:3354) |
Tricho-odonto-onychodysplasia - dominant syndactyly | (Orphanet:3357) |
Triphalangeal thumb - polysyndactyly syndrome | (Orphanet:2950) |
Triploidy | (Orphanet:3376) |
Trisomy 20p | (Orphanet:261318) |
VACTERL/VATER association | (Orphanet:887) |
Van Regemorter-Pierquin-Vamos syndrome | (Orphanet:3419) |
Verloove Vanhorick-Brubakk syndrome | (Orphanet:3429) |
Visceral neuropathy - brain anomalies - facial dysmorphism - developmental delay | (Orphanet:73246) |
WT limb-blood syndrome | (Orphanet:3466) |
Waardenburg syndrome type 3 | (Orphanet:896) |
Weaver syndrome | (Orphanet:3447) |
White forelock with malformations | (Orphanet:2475) |
Zlotogora-Ogur syndrome | (Orphanet:3253) |