Microcephaly 18, Primary, Autosomal Dominant; Mcph18

Table of contents:

Description
Related genes
Clinical Features
Incidence and onset information
Alternative Names
Researches and researchers
Gene Panels
Sources and references

Genes related to Microcephaly 18, Primary, Autosomal Dominant; Mcph18

WDFY3

View recommended genes panels

Clinical Features

Phenotypes and symptoms related to Microcephaly 18, Primary, Autosomal Dominant; Mcph18

Intellectual disability
Microcephaly

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— No data available about the known clinical features onset.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Microcephaly 18, Primary, Autosomal Dominant; Mcph18 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Autism Spectrum Disorders Sequencing Panel with CNV Detection. By PreventionGenetics PreventionGenetics (United States). SCN1A, SCN2A, SGSH, BRAF, SLC6A1, SLC9A6, SPAST, CDKL5, STXBP1, SYN2, TBR1, TCF20, TCF4, TSC1, TSC2, UBE3A, BCL11A, CNTNAP2, CACNA1C, CSMD1 , (...) View the complete list with 85 more genes Panel complete gene list SCN1A, SCN2A, SGSH, BRAF, SLC6A1, SLC9A6, SPAST, CDKL5, STXBP1, SYN2, TBR1, TCF20, TCF4, TSC1, TSC2, UBE3A, BCL11A, CNTNAP2, CACNA1C, CSMD1, NSD1, AUTS2, PCDH19, NLGN4X, NLGN3, SHANK3, SHANK2, DEAF1, CACNA2D3, CTTNBP2, ADNP, TBC1D20, RAB39B, BCKDK, ZMYND11, CDC42BPB, ARID1B, ARX, MFRP, GRIP1, POGZ, ASH1L, POMGNT1, CHD2, STXBP5, ZNF407, CHD8, UPF3B, MBD5, CHD7, WDFY3, ANKRD11, CNTN6, VPS13B, MED13L, DGAT2L6, KMT5B, EHMT1, CTNND2, KATNAL2, CUL3, SETD5, PTCHD1, DHCR7, DISC1, EFR3A, ADSL, TNRC6B, ASXL3, NEXMIF, C12orf57, PACS1, CC2D1A, DSCAM, NAA15, DYRK1A, ABCA7, FMR1, FOLR1, FOXG1, FOXP1, GABRB3, GAMT, GATM, GRIN2B, HCN1, ANK2, HOXA1, KCNQ3, KRAS, SMAD4, MAGEL2, MAOA, MECP2, MYO9B, MYT1L, NDP, NFIX, NRXN1, KAT2B, PQBP1, PTEN, RAD21, RAI1, RELN Specificity 1 % Genes 100 %
WDFY3. By Fulgent Genetics Fulgent Genetics (United States). WDFY3 Specificity 100 % Genes 100 %

Panel Name, Specifity and genes Tested/covered

Autism Spectrum Disorders Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics (United States).

SCN1A, SCN2A, SGSH, BRAF, SLC6A1, SLC9A6, SPAST, CDKL5, STXBP1, SYN2, TBR1, TCF20, TCF4, TSC1, TSC2, UBE3A, BCL11A, CNTNAP2, CACNA1C, CSMD1 , (...)

View the complete list with 85 more genes

Specificity
1 %

Genes
100 %

WDFY3.

By Fulgent Genetics Fulgent Genetics (United States).

WDFY3

Specificity
100 %

Genes
100 %

You can get up to -6 more panels with our dedicated tool

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Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Symptoms Checker

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