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Diseases
Genes (1334)
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FRAS1
Hypertelorism
Microphthalmia
Fraser Syndrome
FREM2
Hypertelorism
Microphthalmia
Fraser Syndrome
GRIP1
Hypertelorism
Microphthalmia
Fraser Syndrome
TBP
Spinocerebellar Ataxia Type 17
FOXP2
Foxp2-Related Speech And Language Disorder
ADGRG1
Bilateral Frontoparietal Polymicrogyria
FOXG1
Foxg1 Syndrome
LMNA
Vocal Cord Paralysis
Hypertelorism
Nemaline Myopathy
Charcot-Marie-Tooth Disease
PMP22
Vocal Cord Paralysis
Charcot-Marie-Tooth Disease
TRPM6
Primary Hypomagnesemia With Secondary Hypocalcemia
MGP
Keutel Syndrome
GDAP1
Vocal Cord Paralysis
Charcot-Marie-Tooth Disease
FIG4
Hypertelorism
Charcot-Marie-Tooth Disease
MPZ
Charcot-Marie-Tooth Disease
TAF1
Mental Retardation, X-Linked, Syndromic 33
IFIH1
Singleton Merten Syndrome
LRSAM1
Charcot-Marie-Tooth Disease
PRSS56
Microphthalmia
COX4I2
Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, And Calvarial Hyperostosis
RB1
Pinealoblastoma
Hypertelorism
Microphthalmia
Trilateral Retinoblastoma