RS797044916 CDC42
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Neurodevelopmental disorder
Postnatal growth retardation
Abnormality of blood and blood-forming tissues
Neurodevelopmental abnormality
Abnormal facial shape
Abnormality of the immune system
Macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome
CDC42-related disorder
Inborn genetic diseases
Neurodevelopmental disorder
Postnatal growth retardation
Abnormality of blood and blood-forming tissues
Neurodevelopmental abnormality
Abnormal facial shape
Other Variants in CDC42