Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome

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Subtype of: Microcephaly
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Pathways column key: KEGG Reactome
Disease terms Disease ID Gene Symbol Classification References Source Pathways
  • microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome
MONDO_0020647
CTU2 Causal
26633546 27480277 31301155
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome.
5 View disease cluster →
Congenital anomalies of the kidney and urinary tract 1 shared geneCTU2 Related via 1 shared gene including CTU2. Microcephaly 1 shared geneCTU2 Related via 1 shared gene including CTU2. Seizures 1 shared geneCTU2 Related via 1 shared gene including CTU2. Breast neoplasms 1 shared geneCTU2 Related via 1 shared gene including CTU2. Autism 1 shared geneCTU2 Related via 1 shared gene including CTU2.