Select item 337637 Spinocerebellar ataxia type 17 Cerebelloparenchymal disorder II HUNTINGTON DISEASE-LIKE 4 Olivopontocerebellar atrophy 5 Olivopontocerebellar atrophy V SCA 17 Spinocerebellar Ataxia Type17 Select item 419034 Hereditary spastic paraplegia 17 Autosomal dominant spastic paraplegia type 17 Silver Syndrome Silver spastic paraplegia syndrome Spastic paraplegia 17 Spastic paraplegia with amyotrophy of hands and feet Select item 1826039 Partial duplication of the short arm of chromosome 17 Select item 1825963 Partial deletion of chromosome 17 Select item 1826046 Partial deletion of the long arm of chromosome 17 Select item 350942 Autosomal dominant nonsyndromic hearing loss 17 Autosomal dominant nonsyndromic deafness 17 DFNA17 Nonsyndromic Hearing Loss and Deafness Deafness, autosomal dominant 17 Deafness, autosomal dominant nonsyndromic sensorineural 17 Late-onset progressive hereditary hearing impairment due to cochleosaccular degeneration Nonsyndromic hereditary deafness DFNA17 Select item 762261 Primary ciliary dyskinesia 17 CILIARY DYSKINESIA, PRIMARY, 17, WITH OR WITHOUT SITUS INVERSUS Primary Ciliary Dyskinesia17: CCDC103-Related Primary Ciliary Dyskinesia Select item 1842221 Chromosome 17p deletion Chromosome 17, deletion Interstitial deletion 17p Partial monosomy of the short arm of chromosome 17 Select item 1826032 Partial duplication of the long arm of chromosome 17 Chromosome 17, trisomy 17q22 Duplication 17q Trisomy 17q22 Select item 318833 Frontotemporal dementia and/or amyotrophic lateral sclerosis 7 AMYOTROPHIC LATERAL SCLEROSIS, CHMP2B-RELATED Amyotrophic lateral sclerosis 17 CHMP2B-related frontotemporal dementia Frontotemporal dementia, chromosome 3-linked Select item 781653 HSD10 mitochondrial disease 17 beta-hydroxysteroid dehydrogenase type 10 deficiency 17-beta-hydroxysteroid dehydrogenase X deficiency 2-methyl-3-hydroxybutyric aciduria 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency 2M3HBA 3-hydroxy-2-methylbutyryl-CoA dehydrogenase deficiency 3H2MBD deficiency Chorioathetosis with Mental Retardation and Abnormal Behavior HSD10 deficiency HSD10 disease HSD17B10 DEFICIENCY Hydroxyacyl-CoA dehydrogenase II deficiency Select item 322153 Retinitis pigmentosa 17 Select item 766178 Joubert syndrome 17 C5orf42-Related Joubert Syndrome Select item 462339 Autosomal recessive limb-girdle muscular dystrophy type 2Q Limb-girdle muscular dystrophy, type 2Q MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 17 Select item 393230 Stature quantitative trait locus 17 Select item 124377 Charcot-Marie-Tooth disease type 1B CHARCOT-MARIE-TOOTH DISEASE, AUTOSOMAL DOMINANT, WITH FOCALLY FOLDED MYELIN SHEATHS, TYPE 1B CHARCOT-MARIE-TOOTH DISEASE, SLOW NERVE CONDUCTION TYPE, LINKED TO DUFFY CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 1B Charcot-Marie-Tooth disease, demyelinating, type 1b Charcot-Marie-Tooth disease, type IB HEREDITARY MOTOR AND SENSORY NEUROPATHY I HEREDITARY MOTOR AND SENSORY NEUROPATHY IB Hereditary motor and sensory neuropathy 1B Peroneal muscular atrophy Select item 83266 Frontotemporal dementia Dementia, frontotemporal, with or without parkinsonism Dementia, frontotemporal, with parkinsonism FRONTOTEMPORAL LOBAR DEGENERATION WITH TAU INCLUSIONS FRONTOTEMPORAL LOBE DEMENTIA FTLD WITH TAU INCLUSIONS Frontotemporal lobe dementia (FLDEM) Multiple system tauopathy with presenile dementia WILHELMSEN-LYNCH DISEASE frontotemporal dementia with parkinsonism-17 Select item 444124 Chromosome 17, deletion 17q23 q24 Deletion 17q23 q24 Monosomy 17q23 q24 Select item 444010 Potocki-Lupski syndrome CHROMOSOME 17p11.2 DUPLICATION SYNDROME Chromosome 17, trisomy 17p11 2 Duplication 17p11 2 Duplication 17p11.2 syndrome Potocki-Lupski syndrome (dup(17)(p11.2p11.2)) Trisomy 17p11 2 Select item 481763 Parkinson disease 17 
