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*614304 - MICRO RNA 137; MIR137
Cytogenetic locations: 610496
Gene summaries Genetic tests Medical literature
*601890 - PROTEIN-TYROSINE KINASE PTK7; PTK7
Cytogenetic locations: 18882711
#614820 - ALTERNATING HEMIPLEGIA OF CHILDHOOD 2; AHC2
Cytogenetic locations: 24842602
#601338 - CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURAL HEARING LOSS; CAPOS
Cytogenetic locations: 607814
#618383 - NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MOVEMENT ABNORMALITIES, COGNITIVE DECLINE, AND BRAIN ABNORMALITIES; NEDMCB
Cytogenetic locations: 35104841
#178110 - CONTRACTURES, PTERYGIA, AND SPONDYLOCARPOTARSAL FUSION SYNDROME 1A; CPSFS1A
Cytogenetic locations: SHPK
254200 - MYASTHENIA GRAVIS; MG
#128235 - DYSTONIA 12; DYT12
#254110 - MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 8; LGMDR8
Cytogenetic locations: 39634523
%184850 - STIFF-PERSON SYNDROME; SPS
PROGRESSIVE ENCEPHALOMYELITIS WITH RIGIDITY, INCLUDED; PERM, INCLUDED; PER, INCLUDED
*602290 - TRIPARTITE MOTIF-CONTAINING PROTEIN 32; TRIM32
Cytogenetic locations: 15786463
#608099 - MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 3; LGMDR3
Cytogenetic locations: 18285821
*182350 - ATPase, Na+/K+ TRANSPORTING, ALPHA-3 POLYPEPTIDE; ATP1A3
#601003 - BRODY DISEASE; BROD
Cytogenetic locations: SRL
*160720 - MYOSIN, HEAVY CHAIN 3, SKELETAL MUSCLE, EMBRYONIC; MYH3
*108730 - ATPase, Ca(2+)-TRANSPORTING, FAST-TWITCH 1; ATP2A1
SERCA1 TRUNCATED ISOFORM, INCLUDED; S1T, INCLUDED
*159440 - MYELIN PROTEIN ZERO; MPZ
Cytogenetic locations: 11709914
#158900 - FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY, INFANTILE, INCLUDED
Cytogenetic locations: 19593370
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