Cranioectodermal dysplasia

MONDO:0009032

Cranioectodermal dysplasia (CED) is a rare developmental disorder characterized by congenital skeletal and ectodermal defects associated with dysmorphic features, nephronophthisis, hepatic fibrosis and ocular anomalies (mainly retinitis pigmentosa).

Also known as: CED, Sensenbrenner syndrome, cranioectodermal dysplasia

2 clinical trials for this condition and its sub-types, 0 tagged with Cranioectodermal dysplasia itself.

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Where it sits in the disease tree

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Part of

↑ Ectodermal dysplasia syndrome (45) ↑ Inherited renal tubular disease (40) ↑ Syndromic craniosynostosis (22) ↑ Craniosynostosis syndrome, autosomal recessive (2) ↑ Short rib-polydactyly syndrome (2)

Sub-types of Cranioectodermal dysplasia

Cranioectodermal dysplasia 1 0 trials
Cranioectodermal dysplasia 2 0 trials
Cranioectodermal dysplasia 3 0 trials
Cranioectodermal dysplasia 4 0 trials
Cranioectodermal dysplasia 5 0 trials
Cranioectodermal dysplasia 6 0 trials
Short-rib thoracic dysplasia 16 with or without polydactyly 0 trials

Including sub-types (2) Tagged with Cranioectodermal dysplasia (0)

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