Any syndromic microphthalmia in which the cause of the disease is a mutation in the VAX1 gene.
Comprehensive, easy-to-understand information about this condition
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anophthalmia/microphthalmia-esophageal atresia syndrome
MONDO:0008799
COFS syndrome
MONDO:0008926
microphthalmia, syndromic 2
MONDO:0010261
X-linked colobomatous microphthalmia-microcephaly-intellectual disability-short stature syndrome
MONDO:0010485
microphthalmia, syndromic 1
MONDO:0010671
linear skin defects with multiple congenital anomalies
MONDO:0010672