ciliopathy (Q203031)
genetic disease associated with mutations encoding defective proteins, which result in either abnormal function formation or function of cilia
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aliases ciliopathies
description genetic disease associated with mutations encoding defective proteins, which result in either abnormal function formation or function of cilia

External Links
(P486) D000072661
(P557) 29887
(P646) /m/04crk2s
(P672) C16.131.077.245
C16.320.184
(P699) DOID:0060340
(P1550) 363250
(P2892) C4277690
(P5270) MONDO_0005308
(P6366) 2780561973
(P10283) C2910395002
C2780561973
(P11956) 0003900