Okt4 Epitope Deficiency
Table of contents:
Clinical Features
Phenotypes and symptoms related to Okt4 Epitope Deficiency
- Immunodeficiency
- Lymphadenopathy
- Systemic lupus erythematosus
- Abnormality of the thyroid gland
- Graves disease
- Abnormal T cell morphology
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.
Alternative names
Okt4 Epitope Deficiency Is also known as t4 epitope deficiency.
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.Okt4 Epitope Deficiency Recommended genes panels
| Panel Name, Specifity and genes Tested/covered |
|---|
 CD4.
By Fulgent Genetics Fulgent Genetics (United States).
CD4
Specificity
100 %
Genes
100 % |
|
Immune Report Card.
By OmniSeq, Inc. (United States).
CXCL10, STAT1, TBX21, TGFB1, TNF, TNFRSF14, TNFRSF18, CD40, CD27, TNFRSF9, TNFSF4, CD40LG, CCR2, CD163, CD2, CD28, CXCR6, CD38, CD4, CD68 , (...)
View the complete list with 24 more genes
Specificity
3 %
Genes
100 % |
You can get up to -6 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
OMIM Rare Disease Search EngineIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC; HMSN2C BENIGN CHRONIC PEMPHIGUS; BCPM CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2S; CMT2S SEIZURES, CORTICAL BLINDNESS, AND MICROCEPHALY SYNDROME; SCBMS SPINAL MUSCULAR ATROPHY, TYPE III; SMA3 CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS; CAN MEIER-GORLIN SYNDROME 6; MGORS6