1. Mendelian
  2. Rare Diseases
  3. OOCYTE MATURATION DEFECT 2; OOMD2

Oocyte Maturation Defect 2; Oomd2

Table of contents:

Genes related to Oocyte Maturation Defect 2; Oomd2

  • TUBB8

View recommended genes panels

Clinical Features

Phenotypes and symptoms related to Oocyte Maturation Defect 2; Oomd2

  • Infertility
  • Myocardial infarction
  • Female infertility
  • Oocyte arrest at metaphase I

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.

Oocyte Maturation Defect 2; Oomd2 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
TUBB8.

By Fulgent Genetics Fulgent Genetics (United States).

TUBB8
Specificity
100 %
Genes
100 %

You can get up to -7 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

OMIM Genetic Syndrome Finder

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like MICROSPHEROPHAKIA AND/OR MEGALOCORNEA, WITH ECTOPIA LENTIS AND WITH OR WITHOUT SECONDARY GLAUCOMA; MSPKA PFEIFFER SYNDROME TYPE 3 ICHTHYOSIS HYSTRIX, CURTH-MACKLIN TYPE; IHCM FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP1 46,XY PARTIAL GONADAL DYSGENESIS XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG