Índice de enfermedades genéticas ofrecidas por AC Gen Reading Life

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(Recomendable en inglés)

A - B - C - D - E - F - G - H - I - J - K - L - M - N - O - P - Q - R - S - T - U - V - W - X - Y - Z 

Enfermedad/Phenotype	Phenotype MIM number	Simbolo del Gen	Nombre del Gen
Usher syndrome
Usher syndrome, type 1B	276900	MYO7A	myosin VIIA
Usher syndrome, type 1C	276904	USH1C	Usher syndrome 1C (autosomal recessive, severe)
Usher syndrome, type 1D	601067	CDH23	cadherin-related 23
Usher syndrome, type 1D/F digenic	601067	CDH23	cadherin-related 23
Usher syndrome, type 1D/F digenic	601067	PCDH15	protocadherin-related 15
Usher syndrome, type 1F	602083	PCDH15	protocadherin-related 15
Usher syndrome, type 2A	276901	USH2A	Usher syndrome 2A (autosomal recessive, mild)
UV-induced skin damage	266300	MC1R	melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor)