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Diseases
Genes (1206)
Deep Research
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TTPA
Familial Isolated Vitamin E Deficiency
FOXP2
Cholera
Foxp2-Related Speech And Language Disorder
ADGRG1
Bilateral Frontoparietal Polymicrogyria
FOXG1
Foxg1 Syndrome
TAF1
Mental Retardation, X-Linked, Syndromic 33
IFIH1
Singleton Merten Syndrome
PRSS56
Microphthalmia
MSTN
Myostatin-Related Muscle Hypertrophy
COX4I2
Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, And Calvarial Hyperostosis
RB1
Pinealoblastoma
Microphthalmia
Hypertelorism
Trilateral Retinoblastoma
TBR1
Microphthalmia
Hypertelorism
Intellectual Developmental Disorder With Autism And Speech Delay
CD55
Cholera
Protein Losing Enteropathy
MFRP
Microphthalmia
PITX3
Microphthalmia
STRA6
Microphthalmia
SYCP3
Spermatogenesis Arrest
TMEM98
Microphthalmia
HMX1
Microphthalmia
ERCC6
Microphthalmia
EFNB1
Hypertelorism