Connexin 26 (Gap Junction Beta 2) Sequencing
Orderable EAP code:
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Comments:
Requisition required.
Refer to KDL Test Directory for more information.
For shipping information or supplies call KDL Client Services at 855-535-1522.
Synonyms:
Non-Syndromic Hereditary Hearing Loss
GJB2, DFNB1, DFNA3
Chromosomal Microarray – Products of Conception
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Comments:
Requisition required.
Refer to KDL Test Directory for more information.
For shipping information or supplies call KDL Client Services at 855-535-1522.
Synonyms:
aCGH
Array comparative genomic hybridization
Chromosome microarray
Competitive genomic hybridization
SNP Microarray – Products of Conception
Erythrocytosis Panel
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Comments:
Requisition required.
Refer to KDL Test Directory for more information.
For shipping information or supplies call KDL Client Services at 855-535-1522.
If JAK2 V617F is negative, reflexes to JAK2 Exon 12 (Opens in a new window)
Synonyms:
JAK2 V617F
JAK2 Exon 12
Thrombocytosis Panel
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Comments:
Requisition required.
Refer to KDL Test Directory for more information.
For shipping information or supplies call KDL Client Services at 855-535-1522.
Synonyms:
Calreticulin
JAK2 V617F
MPL
Premature Chromatid Separation Analysis
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Comments:
Requisition required.
Refer to KDL Test Directory for more information.
For shipping information or supplies call KDL Client Services at 855-535-1522.
Synonyms:
Chromosome Instability
Roberts syndrome
Heterotaxia Panel
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Comments:
Requisition required.
Refer to KDL Test Directory for more information.
For shipping information or supplies call KDL Client Services at 855-535-1522.
Synonyms:
ACVR2B, CITED2, CRELD1, DNAH11, DNAH5, DNAI1, GATA4, GDF1, LEFTY2, NKX2-5, SHROOM3, SMAD2, ZIC3, FOXH1, NODAL
Chimerism, Sorted Cells DNA
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Comments:
Requisition required.
Refer to KDL Test Directory for more information.
For shipping information or supplies call KDL Client Services at 855-535-1522.
Synonyms:
DNA from sorted cells for chimerism study
Craniosynostosis Panel
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Comments:
Requisition required.
Refer to KDL Test Directory for more information.
For shipping information or supplies call KDL Client Services at 855-535-1522.
Synonyms:
Achondroplasia
Antley-Bixler Syndrome
Apert Syndrome
Baller-Gerold Syndrome
Beare-Stevenson cutis gyrate syndrome
Craniofrontonasal Dysplasia
Craniosynostosis mental retardation syndrome of Lin and Gettig
Crouzons Syndrome
Hunter-McAlpine
Jackson-Weiss Syndrome
Muenke Syndrome
Opitz Trigonocephaly Syndrome
Pfeiffer Syndrome
Pierre Robin Syndrome
POR (Cytochrome P450 Oxidoreductase) deficiency with Antley-Bixler phenotype
Saethre-Chotzen Syndrome
Shprintzen-Goldberg craniosynostosis
ALPL, ALX4, ASXL1, EFNB1, FBN1, FGFR1, FGFR2, FGFR3, IFT122, IFT43, IL11RA, MASP1, MSX2, POR, RAB23, RECQL4, SKI, TGFBR1, TGFBR2, TWIST1, WDR19, WDR35, GLI3
Comprehensive Neuromuscular Panel
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Comments:
Requisition required.
Refer to KDL Test Directory for more information.
For shipping information or supplies call KDL Client Services at 855-535-1522.
Synonyms:
Congenital muscular dystrophy
Emery-Dreifuss muscular dystrophy
Limb-Girdle muscular dystrophy
Neuromuscular disorders
BSCL2, DNM2, IGHMBP2, COL6A1, COL6A2, COL6A3, DAG1, FKRP, FKTN, ISPD, ITGA7, LAMA2, LARGE, POMGNT1, POMT1, POMT2, RYR1, SEPN1, TCAP, ACTA1, BIN1, CFL2, MTM1, NEB, TNNT1, TPM2, TPM3, ANO5, CAPN3, DMD, DYSF, EMD, FHL1, FLNC, GAA, GNE, MYOT, PLEC, SGCA, SGCB, SGCD, SGCG, SYNE1, SYNE2, TTN, VRK1, AMPD1, CHAT, CHRNA1, CHRNB1, CHRND, CHRNE, CHRNG, COLQ, DOK7, GLE1, MTMR14, MUSK, MYH2, PABPN1, PLEKHG5, PMM2, PTRF, PYGM, RAPSN, SCN4A, SGCE, SIL1, TNNI2, TRIM32, LMNA, RYR2, CAV3, LDB3, MYH7, BAG3, CRYAB, DES, VCP
MYD88 Mutation Analysis
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Comments:
Requisition required.
Refer to KDL Test Directory for more information.
For shipping information or supplies call KDL Client Services at 855-535-1522.
Synonyms:
Waldenstroms Macroglobulinemia/lymphoblastic lymphoma
WM/LPL
MGUS