Cranioectodermal Dysplasia 1; Ced1

Description

Cranioectodermal dysplasia (CED), also known as Sensenbrenner syndrome, is an autosomal recessive disorder characterized by sagittal craniosynostosis and facial, ectodermal, and skeletal anomalies (summary by Gilissen et al., 2010). Genetic Heterogeneity of Cranioectodermal DysplasiaCranioectodermal dysplasia-2 (CED2 ) is caused by mutation in the WDR35 gene (OMIM ) on chromosome 2p24; CED3 (OMIM ) is caused by mutation in the IFT43 gene (OMIM ) on chromosome 14q24; and CED4 (OMIM ), is caused by mutation in the WDR19 gene (OMIM ) on chromosome 4p14.

Clinical Features

Top most frequent phenotypes and symptoms related to Cranioectodermal Dysplasia 1; Ced1

  • Global developmental delay
  • Generalized hypotonia
  • Pica
  • Microcephaly
  • Growth delay
  • Nystagmus
  • Epicanthus
  • High palate
  • Hepatomegaly
  • Brachydactyly
And another 88 symptoms. If you need more information about this disease we can help you.
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Incidence and onset information

Not enough data available about incidence and published cases.


Mendelian

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Cranioectodermal Dysplasia 1; Ced1 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Retinitis Pigmentosa Panel.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center in United States.

ABHD12, ZNF513, AIPL1, BEST1, NEUROD1, SPATA7, PRKCG, CHM, RP1, ABCA4, MFRP, ARL6, CEP290, CLRN1, TTC8, USH2A, PRPH2, TULP1, SAG, RPGRIP1 , (...)

View the complete list with 72 more genes
Specificity
2 %
Genes
20 %
Ciliopathies.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

VHL, USH1G, USH1C, INVS, SPATA7, CC2D2A, TMEM67, KCNJ13, NPHP3, NPHP1, MKKS, ADGRV1, CEP290, CLRN1, TTC8, TRIM32, USH2A, NPHP4, PCDH15, TULP1 , (...)

View the complete list with 73 more genes
Specificity
4 %
Genes
60 %
Craniosynostosis.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

RECQL4, ALPL, FBN1, FGFR3, FGFR2, FGFR1, WDR35, RAB23, POR, MSX2, TWIST1, TGFBR1, TGFBR2, SKI, GLI3, WDR19, ALX4, EFNB1, ASXL1, MASP1 , (...)

View the complete list with 3 more genes
Specificity
18 %
Genes
80 %
Nephronophthisis Deletion/Duplication Panel.

By Genetic Services Laboratory University of Chicago in United States.

INVS, TMEM67, NPHP3, NPHP1, CEP290, NPHP4, XPNPEP3, IQCB1, DCDC2, WDR19, SDCCAG8, TTC21B, RPGRIP1L, NEK8, GLIS2, IFT172, CEP164, ZNF423, CEP83, ANKS6
Specificity
5 %
Genes
20 %
Renal Cystic Disorders Sequencing Panel.

By Genetic Services Laboratory University of Chicago in United States.

VHL, INVS, HNF1B, INPP5E, CC2D2A, JAG1, TMEM67, ARL6, NPHP3, NPHP1, MKKS, CEP290, TTC8, TRIM32, NPHP4, XPNPEP3, IQCB1, BBS7, BBS5, BBS12 , (...)

View the complete list with 55 more genes
Specificity
2 %
Genes
20 %
Nephronophthisis Sequencing Panel.

By Genetic Services Laboratory University of Chicago in United States.

INVS, TMEM67, NPHP3, NPHP1, CEP290, NPHP4, XPNPEP3, IQCB1, DCDC2, WDR19, SDCCAG8, TTC21B, RPGRIP1L, NEK8, GLIS2, IFT172, CEP164, ZNF423, CEP83, ANKS6
Specificity
5 %
Genes
20 %
Craniofacial Sequencing Panel.

By Genetic Services Laboratory University of Chicago in United States.

RECQL4, FAM20C, FGFR3, RUNX2, FGFR2, FGFR1, FLNA, WDR35, RAB23, POR, MSX2, TWIST1, TGFBR1, TGFBR2, SKI, GLI3, WDR19, ALX4, EFNB1, IFT43 , (...)

View the complete list with 11 more genes
Specificity
13 %
Genes
80 %
Craniofacial Deletion/Duplication Panel.

By Genetic Services Laboratory University of Chicago in United States.

RECQL4, FAM20C, FGFR3, RUNX2, FGFR2, FGFR1, FLNA, WDR35, RAB23, POR, MSX2, TWIST1, TGFBR1, TGFBR2, SKI, GLI3, WDR19, ALX4, EFNB1, IFT43 , (...)

View the complete list with 11 more genes
Specificity
13 %
Genes
80 %
Skeletal Dysplasia Panel, Sequencing (39 Genes) and Deletion/Duplication (36 Genes).

By ARUP Laboratories, Molecular Genetics and Genomics in United States.

ALPL, FKBP10, COL2A1, COL1A1, COL1A2, P3H1, CRTAP, AGPS, PPIB, FGFR3, RUNX2, FGFR2, PEX7, SLC26A2, TRPV4, FGFR1, HSPG2, FLNA, LBR, WDR35 , (...)

View the complete list with 19 more genes
Specificity
6 %
Genes
40 %
Skeletal Dysplasia Panel, Sequencing (39 Genes) and Deletion/Duplication (36 Genes), Fetal.

By ARUP Laboratories, Molecular Genetics and Genomics in United States.

ALPL, FKBP10, COL2A1, COL1A1, COL1A2, P3H1, CRTAP, AGPS, PPIB, FGFR3, RUNX2, FGFR2, PEX7, SLC26A2, TRPV4, FGFR1, HSPG2, FLNA, LBR, WDR35 , (...)

View the complete list with 19 more genes
Specificity
6 %
Genes
40 %
Craniosynostosis.

By Human Genetics Laboratory, Munroe-Meyer Institute University of Nebraska Medical Center in United States.

RECQL4, FGFR3, RUNX2, FGFR2, FGFR1, WDR35, RAB23, POR, MSX2, TWIST1, TGFBR1, TGFBR2, SKI, GLI3, WDR19, EFNB1, ASXL1, IFT43, IL11RA, IFT122 , (...)

View the complete list with 6 more genes
Specificity
16 %
Genes
80 %
WDR19. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

WDR19
Specificity
100 %
Genes
20 %
Craniofacial Del/Dup Panel.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

RECQL4, ALPL, EYA1, DHODH, CHD7, RUNX2, PRKAR1A, SALL1, POLR1C, SIX5, TCOF1, SIX1, POLR1D, WDR35, RAB23, POR, MSX2, TWIST1, SKI, GLI3 , (...)

View the complete list with 23 more genes
Specificity
10 %
Genes
80 %
Craniofacial Seq + Del/Dup Panel.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

RECQL4, ALPL, EYA1, DHODH, CHD7, RUNX2, PRKAR1A, SALL1, POLR1C, SIX5, TCOF1, SIX1, POLR1D, WDR35, RAB23, POR, MSX2, TWIST1, SKI, GLI3 , (...)

View the complete list with 23 more genes
Specificity
10 %
Genes
80 %
Craniofacial Seq Analysis.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

RECQL4, ALPL, EYA1, DHODH, CHD7, RUNX2, PRKAR1A, SALL1, POLR1C, SIX5, TCOF1, SIX1, POLR1D, WDR35, RAB23, POR, MSX2, TWIST1, SKI, GLI3 , (...)

View the complete list with 23 more genes
Specificity
10 %
Genes
80 %
Asphyxiating thoracic dystrophy 5 (sequence analysis of WDR19 gene).

By CGC Genetics in Portugal.

WDR19
Specificity
100 %
Genes
20 %
Craniosynostosis (NGS panel for 30 genes).

By CGC Genetics in Portugal.

RECQL4, ALPL, FGFR3, FGFR2, FGFR1, WDR35, RAB23, POR, TWIST1, TGFBR1, TGFBR2, SKI, GLI3, IFT140, WDR19, SCARF2, ALX4, EFNB1, MASP1, IL11RA , (...)

View the complete list with 10 more genes
Specificity
10 %
Genes
60 %
Nephronophthisis (NGS panel for 19 genes).

By CGC Genetics in Portugal.

INVS, TMEM67, NPHP3, NPHP1, CEP290, NPHP4, XPNPEP3, IQCB1, DCDC2, WDR19, SDCCAG8, TTC21B, RPGRIP1L, NEK8, GLIS2, CEP164, ZNF423, CEP83, ANKS6
Specificity
6 %
Genes
20 %
Ciliopathies (NGS panel for 90 genes).

By CGC Genetics in Portugal.

INVS, INPP5E, CC2D2A, TMEM67, ARL6, NPHP3, NPHP1, MKKS, CEP290, TTC8, TRIM32, NPHP4, CCDC39, CCDC28B, XPNPEP3, IQCB1, BBS7, BBS5, BBS12, MKS1 , (...)

View the complete list with 70 more genes
Specificity
2 %
Genes
20 %
Ellis Van Creveld syndrome (NGS panel for 12 genes).

By CGC Genetics in Portugal.

WDR35, IFT140, WDR19, TTC21B, IFT80, EVC, EVC2, IFT172, DYNC2H1, NEK1, WDR60, WDR34
Specificity
17 %
Genes
40 %
Short-rib thoracic dysplasia, with or without polydactyly (NGS panel for 16 genes).

By CGC Genetics in Portugal.

WDR35, IFT140, WDR19, TTC21B, IFT43, IFT80, EVC, EVC2, IFT122, IFT172, CEP120, CSPP1, DYNC2H1, NEK1, WDR60, WDR34
Specificity
25 %
Genes
80 %
Cranioectodermal dysplasia (NGS panel for 4 genes).

By CGC Genetics in Portugal.

WDR35, WDR19, IFT43, IFT122
Specificity
100 %
Genes
80 %
Nephronophthisis and Senior-Loken Syndrome Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

INVS, TMEM67, NPHP3, NPHP1, CEP290, NPHP4, IQCB1, DCDC2, WDR19, SDCCAG8, TTC21B, RPGRIP1L, NEK8, GLIS2, CEP164, ZNF423, CEP83, ANKS6
Specificity
6 %
Genes
20 %
Short Rib Skeletal Dysplasia Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

FGFR3, FGFR2, SLC26A2, WDR35, SOX9, IFT140, WDR19, TTC21B, IFT80, EVC, EVC2, IFT122, TCTN3, IFT172, DYNC2H1, NEK1, WDR60, WDR34, PAPSS2
Specificity
16 %
Genes
60 %
Skeletal Disorders and Joint Problems Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

RECQL4, ALPL, ANKH, TYROBP, FKBP10, B4GALT7, IFITM5, LRP5, COL2A1, COL1A1, COL1A2, COL3A1, SOST, TGFB1, LEMD3, TNFRSF11A, CLCN7, SHH, FBN1, DHODH , (...)

View the complete list with 238 more genes
Specificity
2 %
Genes
60 %
Comprehensive Inherited Retinal Dystrophies (includes RPGR ORF15) Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

ABHD12, ZNF513, AIPL1, USH1G, USH1C, BEST1, C12orf65, INVS, NEUROD1, SPATA7, MMACHC, FBLN5, LRP5, COL2A1, PRKCG, CHM, PDZD7, RP1, INPP5E, AMACR , (...)

View the complete list with 285 more genes
Specificity
1 %
Genes
60 %
Ciliopathy Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

INVS, INPP5E, CC2D2A, TMEM67, ARL6, NPHP3, NPHP1, MKKS, CEP290, TTC8, TRIM32, NPHP4, RPGR, CCDC39, IQCB1, BBS7, BBS5, BBS12, MKS1, BBS9 , (...)

View the complete list with 73 more genes
Specificity
2 %
Genes
20 %
Hereditary Cystic Kidney Diseases Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

VHL, INVS, LRP5, HNF1B, JAG1, TMEM67, NPHP3, NPHP1, CEP290, NPHP4, IQCB1, PAX2, TSC2, TSC1, PKHD1, UMOD, PKD2, PKD1, COL4A1, OFD1 , (...)

View the complete list with 21 more genes
Specificity
3 %
Genes
20 %
Craniosynostosis Deletion / Duplication panel.

By Connective Tissue Gene Tests in United States.

RECQL4, FGFR3, FGFR2, FGFR1, WDR35, RAB23, POR, MSX2, TWIST1, TGFBR1, TGFBR2, SKI, GLI3, WDR19, EFNB1, IFT43, IL11RA, IFT122, FREM1, CDC45 , (...)

View the complete list with 6 more genes
Specificity
16 %
Genes
80 %
Craniosynostosis Comprehensive panel.

By Connective Tissue Gene Tests in United States.

RECQL4, FGFR3, FGFR2, FGFR1, WDR35, RAB23, POR, MSX2, TWIST1, TGFBR1, TGFBR2, SKI, GLI3, WDR19, EFNB1, IFT43, IL11RA, IFT122, FREM1, CDC45 , (...)

View the complete list with 6 more genes
Specificity
16 %
Genes
80 %
Craniosynostosis NGS panel.

By Connective Tissue Gene Tests in United States.

RECQL4, FGFR3, FGFR2, FGFR1, WDR35, RAB23, POR, MSX2, TWIST1, TGFBR1, TGFBR2, SKI, GLI3, WDR19, EFNB1, IFT43, IL11RA, IFT122, FREM1, CDC45 , (...)

View the complete list with 6 more genes
Specificity
16 %
Genes
80 %
Skeletal dysplasia ciliopathy Deletion / Duplication panel.

By Connective Tissue Gene Tests in United States.

KIAA0586, WDR35, CFAP410, IFT140, WDR19, TTC21B, IFT43, IFT80, EVC, EVC2, IFT122, C2CD3, IFT172, CEP120, DYNC2H1, ICK, NEK1, WDR60, WDR34, IFT81 , (...)

View the complete list with 4 more genes
Specificity
21 %
Genes
100 %
Skeletal dysplasia ciliopathy NGS panel.

By Connective Tissue Gene Tests in United States.

KIAA0586, WDR35, CFAP410, IFT140, WDR19, TTC21B, IFT43, IFT80, EVC, EVC2, IFT122, C2CD3, IFT172, CEP120, DYNC2H1, ICK, NEK1, WDR60, WDR34, IFT81 , (...)

View the complete list with 4 more genes
Specificity
21 %
Genes
100 %
Skeletal dysplasia ciliopathy Comprehensive panel.

By Connective Tissue Gene Tests in United States.

KIAA0586, WDR35, CFAP410, IFT140, WDR19, TTC21B, IFT43, IFT80, EVC, EVC2, IFT122, C2CD3, IFT172, CEP120, DYNC2H1, ICK, NEK1, WDR60, WDR34, IFT81 , (...)

View the complete list with 4 more genes
Specificity
21 %
Genes
100 %
Nephronophthisis and related disorders NGS panel.

By Connective Tissue Gene Tests in United States.

INVS, CC2D2A, TMEM67, NPHP3, NPHP1, CEP290, NPHP4, XPNPEP3, IQCB1, PKHD1, TMEM216, AHI1, OFD1, DCDC2, WDR19, SDCCAG8, TTC21B, TMEM138, RPGRIP1L, NEK8 , (...)

View the complete list with 9 more genes
Specificity
4 %
Genes
20 %
Nephronophthisis and related disorders Comprehensive panel.

By Connective Tissue Gene Tests in United States.

INVS, CC2D2A, TMEM67, NPHP3, NPHP1, CEP290, NPHP4, XPNPEP3, IQCB1, PKHD1, TMEM216, AHI1, OFD1, DCDC2, WDR19, SDCCAG8, TTC21B, TMEM138, RPGRIP1L, NEK8 , (...)

View the complete list with 9 more genes
Specificity
4 %
Genes
20 %
Nephronophthisis and related disorders Deletion / Duplication panel.

By Connective Tissue Gene Tests in United States.

INVS, CC2D2A, TMEM67, NPHP3, NPHP1, CEP290, NPHP4, XPNPEP3, IQCB1, PKHD1, TMEM216, AHI1, OFD1, DCDC2, WDR19, SDCCAG8, TTC21B, TMEM138, RPGRIP1L, NEK8 , (...)

View the complete list with 9 more genes
Specificity
4 %
Genes
20 %
Hereditary kidney disorders - different panels.

By Institute of Human Genetics Cologne University in Germany.

VHL, ACAT1, ARG1, ATP7B, AUH, BCS1L, INVS, HNF1A, MMACHC, EYA1, LRP5, SLC34A1, WT1, PAX6, SDHAF2, HNF1B, RET, INPP5E, CPS1, GLB1 , (...)

View the complete list with 391 more genes
Specificity
2 %
Genes
100 %
Senior Loken Syndrome Panel.

By CeGaT GmbH in Germany.

INVS, NPHP3, NPHP1, CEP290, NPHP4, IQCB1, WDR19, SDCCAG8, CEP164, ZNF423, IFT81, TRAF3IP1
Specificity
9 %
Genes
20 %
Ectodermal dysplasia (including hypotrichosis and hypoplastic hair) Panel.

By CeGaT GmbH in Germany.

BCS1L, DSP, FGFR3, GJB6, PORCN, SHOC2, FGFR2, OFD1, GRHL2, WDR35, SOX18, CTSC, TP63, CDH3, WDR19, FGF10, GJA1, IFT43, IFT122, AXIN2 , (...)

View the complete list with 35 more genes
Specificity
8 %
Genes
80 %
Nephronophthisis Panel.

By CeGaT GmbH in Germany.

INVS, TMEM67, NPHP3, NPHP1, CEP290, NPHP4, XPNPEP3, IQCB1, DCDC2, WDR19, TTC21B, NEK8, GLIS2, CEP164, ZNF423, CEP83, ANKS6, FAN1, SLC41A1
Specificity
6 %
Genes
20 %
Senior Loken Syndrome Panel.

By CeGaT GmbH in Germany.

INVS, NPHP3, NPHP1, CEP290, NPHP4, IQCB1, WDR19, SDCCAG8, CEP164, ZNF423, IFT81, TRAF3IP1
Specificity
9 %
Genes
20 %
Senior-Loken Syndrome Panel.

By CeGaT GmbH in Germany.

INVS, NPHP3, NPHP1, CEP290, NPHP4, IQCB1, WDR19, SDCCAG8, CEP164, ZNF423, IFT81, TRAF3IP1
Specificity
9 %
Genes
20 %
Short-rib dysplasia Panel.

By CeGaT GmbH in Germany.

WDR35, IFT140, WDR19, TTC21B, IFT80, EVC, EVC2, IFT122, IFT172, DYNC2H1, NEK1, WDR60, WDR34
Specificity
24 %
Genes
60 %
Craniosynostosis syndromes Panel.

By CeGaT GmbH in Germany.

RECQL4, FGFR3, FGFR2, FGFR1, WDR35, RAB23, POR, MSX2, TWIST1, SKI, WDR19, ALX4, EFNB1, IFT43, IL11RA, IFT122, FREM1, MEGF8, ERF, TCF12
Specificity
20 %
Genes
80 %
Skeletal Ciliopathies.

By Asper Biogene Asper Biogene LLC in Estonia.

FGFR3, KIAA0586, WDR35, COMP, IFT140, WDR19, TTC21B, IFT43, IFT80, EVC, EVC2, IFT122, TCTN3, IFT172, CEP120, CSPP1, DYNC2H1, NEK1, WDR60, WDR34 , (...)

View the complete list with 3 more genes
Specificity
22 %
Genes
100 %
Eye diseases comprehensive panel.

By Asper Biogene Asper Biogene LLC in Estonia.

ABHD12, ZNF513, AIPL1, USH1G, USH1C, BEST1, INVS, OPN1MW, SPATA7, TYRP1, LRP5, COL2A1, VSX1, SLC45A2, PAX6, ZEB1, CHM, TGFBI, PITX3, TYR , (...)

View the complete list with 255 more genes
Specificity
1 %
Genes
20 %
Retinal Dystrophy Panel.

By Molecular Vision Laboratory in United States.

ABHD12, ZNF513, AIPL1, USH1G, USH1C, BEST1, C12orf65, INVS, OPN1MW, OPN1LW, NEUROD1, SPATA7, MMACHC, LRP5, CHM, PDZD7, RP1, INPP5E, AMACR, OPA1 , (...)

View the complete list with 267 more genes
Specificity
1 %
Genes
20 %
MVL Vision Panel.

By Molecular Vision Laboratory in United States.

ZNF513, USH1G, USH1C, BEST1, C12orf65, INVS, OPN1MW, OPN1LW, NEUROD1, SPATA7, MMACHC, LRP5, CHM, PDZD7, RP1, INPP5E, OPA1, WFS1, CC2D2A, ELOVL4 , (...)

View the complete list with 248 more genes
Specificity
1 %
Genes
20 %
qGenEx Craniofacial Anomalies.

By Quantitative Genomic Medicine Laboratories, SL in Spain.

RECQL4, EYA1, COL2A1, PAX6, FOXC1, PITX2, OTX2, SHH, DHODH, BCOR, CTSK, FGFR3, CHD7, GJB6, IKBKG, PORCN, RUNX2, FGFR2, RAD21, SMC3 , (...)

View the complete list with 116 more genes
Specificity
3 %
Genes
80 %
Invitae Senior-Loken Syndrome Panel.

By Invitae in United States.

INVS, NPHP3, NPHP1, CEP290, NPHP4, IQCB1, WDR19, SDCCAG8
Specificity
13 %
Genes
20 %
Invitae Nephronophthisis Panel.

By Invitae in United States.

INVS, CC2D2A, TMEM67, NPHP3, NPHP1, CEP290, NPHP4, XPNPEP3, IQCB1, PKHD1, TMEM216, AHI1, OFD1, DCDC2, WDR19, SDCCAG8, TTC21B, TMEM237, TCTN1, RPGRIP1L , (...)

View the complete list with 7 more genes
Specificity
4 %
Genes
20 %
Invitae Ciliopathies Panel.

By Invitae in United States.

INVS, INPP5E, CC2D2A, TMEM67, ARL6, NPHP3, NPHP1, MKKS, CEP290, TTC8, TRIM32, NPHP4, RPGR, CCDC39, XPNPEP3, IQCB1, BBS7, BBS5, BBS12, MKS1 , (...)

View the complete list with 82 more genes
Specificity
3 %
Genes
60 %
Invitae Skeletal Ciliopathies Panel.

By Invitae in United States.

KIAA0586, WDR35, IFT140, WDR19, TTC21B, IFT80, EVC, EVC2, IFT122, TCTN3, IFT172, CEP120, CSPP1, DYNC2H1, NEK1, WDR60, WDR34
Specificity
18 %
Genes
60 %
Craniosysostosis.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

RECQL4, FGFR3, FGFR2, FGFR1, WDR35, RAB23, POR, MSX2, TWIST1, TGFBR1, TGFBR2, SKI, GLI3, WDR19, EFNB1, IFT43, IL11RA, IFT122, FREM1
Specificity
22 %
Genes
80 %
Jeune asphyxiating thoracic dystrophy.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

WDR19, TTC21B, IFT80, DYNC2H1
Specificity
25 %
Genes
20 %
Ciliopathies: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

VHL, AIPL1, USH1G, USH1C, INVS, SPATA7, CC2D2A, TMEM67, KCNJ13, ARL6, NPHP3, NPHP1, MKKS, ADGRV1, CEP290, CLRN1, TTC8, TRIM32, USH2A, NPHP4 , (...)

View the complete list with 92 more genes
Specificity
3 %
Genes
60 %
Ciliopathies: Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

VHL, AIPL1, USH1G, USH1C, INVS, SPATA7, CC2D2A, TMEM67, KCNJ13, ARL6, NPHP3, NPHP1, MKKS, ADGRV1, CEP290, CLRN1, TTC8, TRIM32, USH2A, NPHP4 , (...)

View the complete list with 76 more genes
Specificity
4 %
Genes
60 %
Ciliopathies NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

VHL, AIPL1, USH1G, USH1C, INVS, SPATA7, CC2D2A, TMEM67, KCNJ13, ARL6, NPHP3, NPHP1, MKKS, ADGRV1, CEP290, CLRN1, TTC8, TRIM32, USH2A, NPHP4 , (...)

View the complete list with 75 more genes
Specificity
4 %
Genes
60 %
WDR19.

By Fulgent Genetics Fulgent Genetics in United States.

WDR19
Specificity
100 %
Genes
20 %
KidneySeq - 264 Genes.

By Iowa Institute of Human Genetics University of Iowa in United States.

TTR, VHL, ATP7B, INVS, EYA1, SLC34A1, WT1, HNF1B, RET, INPP5E, CC2D2A, OCRL, JAG1, HPRT1, TMEM67, ARL6, NPHP3, NPHP1, MKKS, CEP290 , (...)

View the complete list with 232 more genes
Specificity
2 %
Genes
80 %
Nephronophthisis Panel.

By Blueprint Genetics in Finland.

INVS, TMEM67, NPHP3, NPHP1, CEP290, NPHP4, IQCB1, DCDC2, WDR19, SDCCAG8, TTC21B, RPGRIP1L, NEK8, GLIS2, IFT172, CEP164, ZNF423, CEP83, ANKS6, MAPKBP1
Specificity
5 %
Genes
20 %
Cystic Kidney Disease Panel.

By Blueprint Genetics in Finland.

VHL, INVS, EYA1, LRP5, HNF1B, JAG1, TMEM67, NPHP3, NPHP1, CEP290, NPHP4, IQCB1, PAX2, TSC2, TSC1, PKHD1, UMOD, PKD2, PKD1, COL4A1 , (...)

View the complete list with 20 more genes
Specificity
3 %
Genes
20 %
Retinal Dystrophy Panel.

By Blueprint Genetics in Finland.

ABHD12, ZNF513, AIPL1, USH1G, USH1C, BEST1, INVS, SPATA7, MMACHC, LRP5, COL2A1, PRKCG, CHM, PDZD7, RP1, INPP5E, OPA1, WFS1, CC2D2A, ELOVL4 , (...)

View the complete list with 240 more genes
Specificity
1 %
Genes
20 %
Short Rib Dysplasia / Asphyxiating Thoracic Dysplasia Panel.

By Blueprint Genetics in Finland.

WDR35, GLI2, IFT140, WDR19, TTC21B, IFT80, EVC, EVC2, IFT122, TCTN3, IFT172, CSPP1, DYNC2H1, NEK1, WDR60, WDR34
Specificity
19 %
Genes
60 %
Retinitis Pigmentosa Panel.

By Blueprint Genetics in Finland.

ABHD12, ZNF513, AIPL1, USH1C, BEST1, SPATA7, PRKCG, CHM, RP1, INPP5E, ABCA4, MFRP, ARL6, CEP290, CLRN1, TTC8, USH2A, PRPH2, TULP1, SAG , (...)

View the complete list with 90 more genes
Specificity
1 %
Genes
20 %
Craniosynostosis Panel.

By Blueprint Genetics in Finland.

RECQL4, ALPL, FGFR3, FGFR2, FGFR1, PAX3, EDNRB, SOX10, WDR35, RAB23, POR, MSX2, TWIST1, TGFBR1, TGFBR2, SKI, GLI3, IFT140, WDR19, ALX4 , (...)

View the complete list with 17 more genes
Specificity
9 %
Genes
60 %
Skeletal Dysplasias Core Panel.

By Blueprint Genetics in Finland.

ALPL, ANKH, FKBP10, LRP5, COL2A1, COL1A1, COL1A2, TGFB1, TNFRSF11A, CLCN7, SERPINF1, SLC39A13, P3H1, CRTAP, PLOD2, AGPS, CTSK, CYP27B1, FAM20C, CA2 , (...)

View the complete list with 91 more genes
Specificity
2 %
Genes
40 %
Comprehensive Skeletal Dysplasias and Disorders Panel.

By Blueprint Genetics in Finland.

RECQL4, ALPL, ANKH, TYROBP, FKBP10, B4GALT7, LRP5, COL2A1, COL1A1, COL1A2, SOST, TGFB1, LEMD3, TNFRSF11A, PYCR1, CLCN7, ATP6V0A2, FBN1, SERPINF1, SP7 , (...)

View the complete list with 226 more genes
Specificity
2 %
Genes
80 %
Ciliopathy Panel.

By Blueprint Genetics in Finland.

INVS, INPP5E, CC2D2A, TMEM67, ARL6, NPHP3, NPHP1, MKKS, CEP290, TTC8, TRIM32, NPHP4, C8orf37, IQCB1, PMM2, BBS7, BBS5, BBS12, MKS1, BBS9 , (...)

View the complete list with 79 more genes
Specificity
5 %
Genes
80 %
Micromelic Dysplasia Panel.

By Blueprint Genetics in Finland.

FBN1, FGFR3, SMAD4, PRKAR1A, SHOX, WDR35, SOX9, ADAMTSL2, IFT140, LTBP2, BMPR1B, WDR19, GNAS, IFT122, EXT1, WNT5A, ROR2, LIFR, SLC35D1, TRIP11 , (...)

View the complete list with 7 more genes
Specificity
12 %
Genes
60 %
Congenital Hepatic Fibrosis Panel.

By Blueprint Genetics in Finland.

INVS, INPP5E, CC2D2A, TMEM67, ARL6, NPHP3, NPHP1, MKKS, CEP290, TTC8, TRIM32, NPHP4, IQCB1, BBS7, BBS5, BBS12, MKS1, BBS9, BBS10, BBS4 , (...)

View the complete list with 32 more genes
Specificity
4 %
Genes
40 %
Comprehensive Growth Disorders / Skeletal Dysplasias and Disorders Panel.

By Blueprint Genetics in Finland.

RECQL4, ALPL, ANKH, TYROBP, FKBP10, B4GALT7, BCS1L, IFITM5, LRP5, COL2A1, COL1A1, COL1A2, COL3A1, SOST, TGFB1, LEMD3, TNFRSF11A, PYCR1, CLCN7, ATP6V0A2 , (...)

View the complete list with 288 more genes
Specificity
2 %
Genes
80 %
Jeune syndrome (type 5).

By Bioarray in Spain.

WDR19
Specificity
100 %
Genes
20 %
SHORT-RIB THORACIC DYSPLASIA.

By Laboratorio de Genetica Clinica SL in Spain.

IFT140, WDR19, TTC21B, IFT80, DYNC2H1
Specificity
20 %
Genes
20 %
Newborn Thoracic Dystrophy Type 5, Sequencing WDR19 Gene.

By Reference Laboratory Genetics in Spain.

WDR19
Specificity
100 %
Genes
20 %
Asphyxiating Thoracic Dystrophy , Panel Massive Sequencing (NGS) DYNC2H1,IFT80,TTC21B,WDR19 Genes.

By Reference Laboratory Genetics in Spain.

WDR19, TTC21B, IFT80, DYNC2H1
Specificity
25 %
Genes
20 %
Senior-Loken Syndrome , Panel Massive Sequencing (NGS) 7 Genes.

By Reference Laboratory Genetics in Spain.

NPHP1, CEP290, NPHP4, IQCB1, WDR19, SDCCAG8, TRAF3IP1
Specificity
15 %
Genes
20 %
Non-immune Hydrops Panel.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center in United States.

COL2A1, GNPTAB, GLB1, HADHA, RAF1, SMPD1, RPL35A, HADHB, ALG9, ALG1, CTSA, GUSB, GALNS, GBE1, PMM2, FGFR3, GBA, BRAF, DHCR7, GLA , (...)

View the complete list with 67 more genes
Specificity
2 %
Genes
20 %
Hypospadias Sequencing Panel.

By Genetic Services Laboratory University of Chicago in United States.

WT1, HNF1B, PITX2, MKKS, TMEM70, HSD3B2, CYP11A1, HCCS, BCOR, SOX2, FGFR3, AR, ARX, CREBBP, DHCR7, PTPN11, FGFR2, CDKN1C, GPC3, HBA1 , (...)

View the complete list with 41 more genes
Specificity
2 %
Genes
20 %
Craniosynostosis Sequence Analysis.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

RECQL4, RUNX2, WDR35, RAB23, POR, MSX2, TWIST1, SKI, EFNB1, IFT43, IFT122, SPECC1L, MEGF8, ZIC1, ERF, TCF12, CD96
Specificity
18 %
Genes
60 %
Craniosynostosis Del/Dup Panel.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

RECQL4, RUNX2, WDR35, RAB23, POR, MSX2, TWIST1, SKI, EFNB1, IFT43, IFT122, SPECC1L, MEGF8, ZIC1, ERF, TCF12, CD96
Specificity
18 %
Genes
60 %
Craniosynostosis Seq + Del/Dup Panel.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

RECQL4, RUNX2, WDR35, RAB23, POR, MSX2, TWIST1, SKI, EFNB1, IFT43, IFT122, SPECC1L, MEGF8, ZIC1, ERF, TCF12, CD96
Specificity
18 %
Genes
60 %
Cranioectodermal dysplasia (sequence analysis of WDR35 gene).

By CGC Genetics in Portugal.

WDR35
Specificity
100 %
Genes
20 %
Cranioectodermal Dysplasia 2 (CED2) / Short-Rib Polydactyly Syndromes Type 5 (SRP5) via the WDR35 Gene.

By PreventionGenetics PreventionGenetics in United States.

WDR35
Specificity
100 %
Genes
20 %
Disorders of Sex Development (DSD) and Infertility Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

HFE, FOXL2, STAR, WT1, HNF1B, HSD17B4, PITX2, ARL6, MKKS, TTC8, TRIM32, CYP11B1, TMEM70, HSD3B2, CYP11A1, HCCS, BCOR, CYB5A, GALT, BBS7 , (...)

View the complete list with 186 more genes
Specificity
1 %
Genes
20 %
Disorders of Sex Development (DSD) Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

HFE, FOXL2, STAR, WT1, HNF1B, HSD17B4, PITX2, ARL6, MKKS, TTC8, TRIM32, CYP11B1, TMEM70, HSD3B2, CYP11A1, HCCS, BCOR, CYB5A, BBS7, BBS5 , (...)

View the complete list with 138 more genes
Specificity
1 %
Genes
20 %
Micromelic dysplasia: acromelic, acromesomelic, mesomelic and rhizo-mesomelic dysplasia Panel.

By CeGaT GmbH in Germany.

FBN1, FGFR3, PRKAR1A, WDR35, ADAMTSL2, IFT140, IFT43, IFT122, WNT5A, ROR2, PDE4D, ZSWIM6, GPC6, TRPS1, GDF5, DDR2, NPR2, IHH, GSC
Specificity
16 %
Genes
60 %
Single gene testing WDR35.

By CeGaT GmbH in Germany.

WDR35
Specificity
100 %
Genes
20 %
Disproportionate Short Stature: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

ANKH, COL2A1, COL1A1, FBN1, SLC39A13, AGPS, CTSK, FAM20C, FGFR3, COL10A1, PTPN11, RUNX2, FGFR2, CDKN1C, PRKAR1A, SLC26A2, TRPV4, FGFR1, SHOX, ANO5 , (...)

View the complete list with 65 more genes
Specificity
3 %
Genes
40 %
Skeletal Dysplasia: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

RECQL4, ALPL, ANKH, TYROBP, FKBP10, B4GALT7, IFITM5, LRP5, COL2A1, COL1A1, COL1A2, SOST, TGFB1, LEMD3, TNFRSF11A, PYCR1, CLCN7, CC2D2A, ATP6V0A2, TMEM67 , (...)

View the complete list with 143 more genes
Specificity
2 %
Genes
40 %
Disproportionate Short Stature: Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

ANKH, COL2A1, COL1A1, FBN1, SLC39A13, CTSK, FAM20C, FGFR3, COL10A1, PTPN11, RUNX2, FGFR2, CDKN1C, PRKAR1A, SLC26A2, TRPV4, FGFR1, SHOX, ANO5, HSPG2 , (...)

View the complete list with 56 more genes
Specificity
3 %
Genes
40 %
Skeletal Dysplasias NGS panel.

By Fulgent Genetics Fulgent Genetics in United States.

RECQL4, ALPL, ANKH, TYROBP, FKBP10, B4GALT7, IFITM5, LRP5, COL2A1, COL1A1, COL1A2, SOST, TGFB1, LEMD3, TNFRSF11A, PYCR1, CLCN7, CC2D2A, ATP6V0A2, TMEM67 , (...)

View the complete list with 141 more genes
Specificity
2 %
Genes
40 %
WDR35.

By Fulgent Genetics Fulgent Genetics in United States.

WDR35
Specificity
100 %
Genes
20 %
Ectodermal Dysplasia Panel.

By Blueprint Genetics in Finland.

BCS1L, DSP, GJB2, GJB6, PORCN, RMRP, ERCC2, WDR35, TP63, CDH3, JUP, EVC, EVC2, IFT122, EDA, MPLKIP, EDAR, WNT10A, EDARADD, HR , (...)

View the complete list with 3 more genes
Specificity
9 %
Genes
40 %
Ellis-Van Creveld Syndrome , Panel Massive Sequencing (NGS) 6 Genes.

By Reference Laboratory Genetics in Spain.

WDR35, GLI2, IFT80, EVC, EVC2, DYNC2H1
Specificity
17 %
Genes
20 %
IFT52.

By Fulgent Genetics Fulgent Genetics in United States.

IFT52
Specificity
100 %
Genes
20 %
IFT43.

By Fulgent Genetics Fulgent Genetics in United States.

IFT43
Specificity
100 %
Genes
20 %
Cranioectodermal dysplasia (sequence analysis of IFT122 gene).

By CGC Genetics in Portugal.

IFT122
Specificity
100 %
Genes
20 %
Cranioectodermal Dysplasia 1 (CED1) via the IFT122 Gene.

By PreventionGenetics PreventionGenetics in United States.

IFT122
Specificity
100 %
Genes
20 %
IFT122.

By Fulgent Genetics Fulgent Genetics in United States.

IFT122
Specificity
100 %
Genes
20 %

Alternate names

Cranioectodermal Dysplasia 1; Ced1 Is also known as sensenbrenner syndrome, levin syndrome i;ced; sensenbrenner syndrome.



If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL; HFTC SHORT RIB-POLYDACTYLY SYNDROME, VERMA-NAUMOFF TYPE COLOBOMA, OCULAR, AUTOSOMAL RECESSIVE CILIARY DYSKINESIA, PRIMARY, 17; CILD17 BARRETT ESOPHAGUS

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