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known as Sensenbrenner–Dorst–Owens syndrome,
Levin syndrome I and
cranioectodermal dysplasia (CED)
These are
pleomorphic and include[citation needed]...
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myopathy with
Moebius and
Robin sequences Cornelia de
Lange syndrome 3
Cranioectodermal dysplasia 2
Craniosynostosis (nonsyndromic) 6
Developmental and epileptic...
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syndrome Cowden syndrome Craniodiaphyseal dysplasia,
autosomal dominant Cranioectodermal dysplasia Craniometaphyseal dysplasia Craniosynostosis D-2-hydroxyglutaric...
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syndrome Cardiocranial syndrome,
Pfeiffer type Coffin-Siris
syndrome 7
Cranioectodermal dysplasia 1, 3, and 4
Craniosynostosis (nonsyndromic) 4 Craniosynostosis...
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Lange syndrome 1, 3, and 5
Costello syndrome Cowden syndrome 5 and 6
Cranioectodermal dysplasia 2 and 3
Craniofacial microsomia Cutis laxa,
autosomal recessive...
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dysplasia syndrome Cloverleaf skull-multiple
congenital anomalies syndrome Cranioectodermal dysplasia 2
Crouzon syndrome Micromelic bone
dysplasia with cloverleaf...
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Retrieved 2023-07-05. "
Cranioectodermal dysplasia (Concept Id: C4551571)". www.ncbi.nlm.nih.gov.
Retrieved 2023-07-05. "
Cranioectodermal dysplasia 1 (Concept...
- 266900 NPHP1, NPHP4, IQCB1, CEP290, SDCCAG8 Eye
Sensenbrenner syndrome (
cranioectodermal dysplasia) 218330 IFT122
Short rib–polydactyly
syndrome 613091 DYNC2H1...
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Craniodiaphyseal dysplasia Craniodigital syndrome mental ****ation
Cranioectodermal dysplasia Craniofacial and
osseous defects mental ****ation Craniofacial...
- Beales, P. L., Ropers, H.-H., Latos-Bielenska, A., Kuss, A. W. (2010). "
Cranioectodermal dysplasia,
Sensenbrenner syndrome, is a
ciliopathy caused by mutations...
