Coproporphyria
Gene: CPOX_MLPA
Cornelia de Lange syndrome
Gene: NIPBL_MLPA
Congenital alveolar capillary dysplasia
Gene: FOXF1_MLPA
Cohen syndrome
Gene: VPS13B_MLPA
Coats disease
Gene: NDP_MLPA
Cerebral cavernous malformation, type 3
Gene: PDCD10_MLPA
Cerebral cavernous malformation, type 1
Gene: KRIT1_MLPA
Cerebral cavernous malformation, type 2
Gene: CCM2_MLPA
Caroli disease
Gene: PKHD1_MLPA
Carnitine deficiency, systemic primary
Gene: SLC22A5_MLPA
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