Oocyte Maturation Defect 2; Oomd2
Table of contents:
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 moreSources and references
You can check the following sources for additional information.
OMIM Rare Disease Symptoms CheckerIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like HEMATURIA, BENIGN FAMILIAL; BFH GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF GLUT1 DEFICIENCY SYNDROME 2; GLUT1DS2 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2 BRAIN MALFORMATIONS WITH OR WITHOUT URINARY TRACT DEFECTS; BRMUTD INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL; ILNEB
TUBB8.