chromosome	gene symbol	phenotype
15q	?	Nemaline myopathy -NEM6
15q11-q14	ACTC1 actin, alpha, cardiac muscle precursor	Cardiomyopathy, dilated, 1R -CMD1R Cardiomyopathy, familial hypertrophic -CMH1 Asymmetric septal hypertrophy -ASH
15q11.2	NIPA1 non-imprinted in Prader-Willi/Angelman syndrome 1	Spastic paraplegia 6 uncomplicated,autosomal dominant,Strumpell-Lorrain type -SPG6
15q13-q15	SLC12A6 potassium chloride cotransporter KCC3	Agenesis of the corpus callosum with peripheral neuropathy -ACCPN Charlevoix disease -SLC12A6 Andermann syndrome -SLC12A6
15q14	SPG11 spatacsin	Spastic paraplegia 11 -SPG11
15q14-q21.3	?	-
15q15-q21	?	Amyotrophic lateral sclerosis -ALS5
15q15.1-q21.1	CAPN3 calpain 3	Muscular dystrophy, limb-girdle, type 2A -LGMD2A
15q15.2	TTBK2 tau tubulin kinase 2	Spinocerebellar ataxia 11 -SCA11
15q21-q22	SPG21 maspardin	Spastic paraplegia 20 -SPG21
15q22	TPM1 tropomyosin 1 (alpha)	Cardiomyopathy, familial hypertrophic, 3 -CMH3
15q23-q25	ETFA electron-transfer-flavoprotein, alpha polypeptide	Multiple acyl-CoA dehydrogenase deficiency -MADD
15q24-q26	?	Spinocerebellar ataxia, autosomal recessive 5 -SCAR5
15q24.1	HCN4 hyperpolarization activated cyclic nucleotide-gated potassium channel 4	familial sinusal bradycardia -FSBD Sick Sinus Syndrome 2, autosomal dominant -SSS2
15q25	POLG polymerase (DNA directed), gamma	progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal -PEOA1 sensory ataxic neuropathy, dysarthria, and ophthalmoparesis -SANDO spinocerebellar ataxia with epilepsy, included -SCAE