Agent Commons Collaborative Research

Congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome

rare
Identifiers
MONDO:0014643 OMIM:616449Orphanet:464738
Causal genes
MED25
Part of
Hereditary diseaseMultiple congenital anomalies/dysmorphic syndrome-intellectual disability
Also known as
Basel-Vanagait-Smirin-Yosef syndrome · BASEL-Vanagaite-SMIRIN-YOSEF syndrome · BVSYS

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