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Diseases
Genes (2239)
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PMM2
Pmm2 Deficiency
Hypertelorism
ASL
Tuberculosis
Argininosuccinic Aciduria
FOXP2
Tuberculosis
Foxp2-Related Speech And Language Disorder
FOXG1
Foxg1 Syndrome
ADGRG1
Bilateral Frontoparietal Polymicrogyria
TRPM6
Primary Hypomagnesemia With Secondary Hypocalcemia
ZIC3
Situs Ambiguus
Hypertelorism
MGP
Keutel Syndrome
PRSS56
Microphthalmia
MMP21
Situs Ambiguus
ACVR2B
Situs Ambiguus
SLC11A1
Tuberculosis
COX4I2
Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, And Calvarial Hyperostosis
RB1
Pinealoblastoma
Hypertelorism
Microphthalmia
Trilateral Retinoblastoma
DHX30
Neurodevelopmental Disorder With Severe Motor Impairment And Absent Language
NODAL
Situs Ambiguus
CFAP53
Situs Ambiguus
LEFTY2
Situs Ambiguus
MFRP
Microphthalmia
PITX3
Microphthalmia