Microcephaly 18, Primary, Autosomal Dominant; Mcph18

Clinical Features

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

  • Intellectual disability
  • Microcephaly

Incidence and onset information

Not enough data available about incidence and published cases.


Mendelian

Accelerate your rare disease diagnosis with us

Learn more

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 in United States.

FMR1, UBE3A, PTEN, ADSL, MFRP, NDP, MECP2, GAMT, GATM, STXBP1, MAOA, SLC9A6, SGSH, ARX, BRAF, CDKL5, CHD7, DHCR7, FOXG1, KRAS , (...)

View the complete list with 87 more genes
Specificity
1 %
Genes
100 %
WDFY3.

By Fulgent Genetics Fulgent Genetics in United States.

WDFY3
Specificity
100 %
Genes
100 %


Need help with a diagnosis?

Learn more about how to achieve it with Mendelian


Learn more

Other rare diseases that you may find interesting

SPASTIC PARAPLEGIA 73, AUTOSOMAL DOMINANT; SPG73 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1B; LGMD1B MEACHAM SYNDROME CEROID LIPOFUSCINOSIS, NEURONAL, 4B, AUTOSOMAL DOMINANT; CLN4B FAMILIAL PAPILLARY OR FOLLICULAR THYROID CARCINOMA MITOCHONDRIAL DNA DEPLETION SYNDROME 6 (HEPATOCEREBRAL TYPE); MTDPS6 MYOCLONUS, FAMILIAL CORTICAL; FCM