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bn:01061351n
Noun Concept
SYL
No term available
EN
A ciliopathy is any genetic disorder that affects the cellular cilia or the cilia anchoring structures, the basal bodies, or ciliary function. Wikipedia
Relations
Sources
IS A
EN
rare disease
EN
genetic disease
EN
disease
EN
syndrome
EN
monogenic disease
HAS KIND
EN
Joubert syndrome
EN
Meckel–Gruber syndrome
EN
RHYNS syndrome
EN
primary ciliary dyskinesia
EN
Asphyxiating thoracic dysplasia
GENETIC ASSOCIATION
EN
OFD1
EN
DNAI1
EN
TMEM67
EN
CEP164
EN
DCDC2
HEALTH SPECIALTY
EN
medical genetics

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