Acro-pectoral syndrome
|
(Orphanet:85203)
|
Acro-renal-ocular syndrome
|
(Orphanet:959)
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Acrocallosal syndrome
|
(Orphanet:36)
|
Apert syndrome
|
(Orphanet:87)
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Biemond syndrome type 2
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(Orphanet:141333)
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Bowed tibiae - radial anomalies - osteopenia - fractures
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(Orphanet:3331)
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Brachydactyly - preaxial hallux varus
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(Orphanet:1278)
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Braddock syndrome
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(Orphanet:52047)
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Branchio-oculo-facial syndrome
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(Orphanet:1297)
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CERVICAL RIBS, SPRENGEL ANOMALY, ANAL ATRESIA, AND URETHRAL OBSTRUCTION
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(OMIM:601389)
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CHARGE syndrome
|
(Orphanet:138)
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Curry-Jones syndrome
|
(Orphanet:1553)
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Diabetic embryopathy
|
(Orphanet:1926)
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Femoral-facial syndrome
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(Orphanet:1988)
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Greig cephalopolysyndactyly syndrome
|
(Orphanet:380)
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Hallux varus - preaxial polysyndactyly
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(Orphanet:2110)
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Hydrolethalus
|
(Orphanet:2189)
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Hypertelorism - hypospadias - polysyndactyly syndrome
|
(Orphanet:2211)
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Hypoplastic tibiae - postaxial polydactyly
|
(Orphanet:3332)
|
IVIC syndrome
|
(Orphanet:2307)
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Intellectual deficit, X-linked, Siderius type
|
(Orphanet:85287)
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Joubert syndrome with orofaciodigital defect
|
(Orphanet:2754)
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Lacrimo-auriculo-dento-digital syndrome
|
(Orphanet:2363)
|
Laurin-Sandrow syndrome
|
(Orphanet:2378)
|
Lung agenesis - heart defect - thumb anomalies
|
(Orphanet:1120)
|
MENTAL RETARDATION, MICROCEPHALY, GROWTH RETARDATION, JOINT CONTRACTURES,AND FACIAL DYSMORPHISM
|
(OMIM:606242)
|
MICROCEPHALY, CORPUS CALLOSUM DYSGENESIS, AND CLEFT LIP/PALATE
|
(OMIM:601420)
|
Mandibulofacial dysostosis-microcephaly syndrome
|
(Orphanet:79113)
|
Meckel syndrome
|
(Orphanet:564)
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Microphthalmia with brain and digit anomalies
|
(Orphanet:139471)
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Neuroectodermal syndrome, Johnson type
|
(Orphanet:2316)
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Oculoauriculovertebral spectrum with radial defects
|
(Orphanet:2549)
|
Oculodentodigital dysplasia
|
(Orphanet:2710)
|
Orofaciodigital syndrome type 1
|
(Orphanet:2750)
|
Orofaciodigital syndrome type 10
|
(Orphanet:2756)
|
Orofaciodigital syndrome type 2
|
(Orphanet:2751)
|
Orofaciodigital syndrome type 4
|
(Orphanet:2753)
|
Orofaciodigital syndrome type 5
|
(Orphanet:2919)
|
Polydactyly of a biphalangeal thumb
|
(Orphanet:93339)
|
Polysyndactyly - cardiac malformation
|
(Orphanet:2934)
|
Preaxial polydactyly - colobomata - intellectual deficit
|
(Orphanet:2921)
|
Preaxial polydactyly of toes
|
(Orphanet:295006)
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Rhizomelic syndrome, Urbach type
|
(Orphanet:3098)
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Sakati-Nyhan syndrome
|
(Orphanet:3128)
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Say-Field-Coldwell syndrome
|
(Orphanet:3133)
|
Short rib-polydactyly syndrome
|
(Orphanet:1505)
|
Short rib-polydactyly syndrome, Majewski type
|
(Orphanet:93269)
|
Short rib-polydactyly syndrome, Verma-Naumoff type
|
(Orphanet:93271)
|
Syndactyly-polydactyly-ear lobe syndrome
|
(Orphanet:3259)
|
Synpolydactyly type 1
|
(Orphanet:295195)
|
Thalidomide embryopathy
|
(Orphanet:3312)
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Tibial aplasia - ectrodactyly
|
(Orphanet:3329)
|
Townes-Brocks syndrome
|
(Orphanet:857)
|
Triphalangeal thumb - polysyndactyly syndrome
|
(Orphanet:2950)
|
Trisomy 1q
|
(Orphanet:261344)
|
Trisomy 20p
|
(Orphanet:261318)
|
Trisomy 4p
|
(Orphanet:1738)
|
VACTERL/VATER association
|
(Orphanet:887)
|
Wolf-Hirschhorn syndrome
|
(Orphanet:280)
|