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CEP55

centrosomal protein 55

gene with protein productOMIM: 6100001 заболевание
GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Disease-causing germline mutation(s) (loss of function) in1
Multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndromeORPHA:500135
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Данные: Orphadata (CC-BY-4.0)