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cranioectodermal dysplasia 4

Disease Summary
Associated Targets (1)
Tbio

1


Uniprot Description A disorder primarily characterized by craniofacial, skeletal and ectodermal abnormalities. Clinical features include craniosynostosis, narrow rib cage, short limbs, brachydactyly, hypoplastic and widely spaced teeth, sparse hair, skin laxity and abnormal nails. Nephronophthisis leading to progressive renal failure, hepatic fibrosis, heart defects, and retinitis pigmentosa have also been described.
Mondo Term and Equivalent IDs
MONDO:0013719:  cranioectodermal dysplasia 4
UMLS:C3280616: