Any exudative vitreoretinopathy in which the cause of the disease is a mutation in the NDP gene.
Comprehensive, easy-to-understand information about this condition
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X-linked Opitz G/BBB syndrome
MONDO:0010222
X-linked immunoneurologic disorder
MONDO:0010243
X-linked adrenal hypoplasia congenita
MONDO:0010264
X-linked lissencephaly with abnormal genitalia
MONDO:0010268
X-linked severe congenital neutropenia
MONDO:0010294
X-linked distal spinal muscular atrophy type 3
MONDO:0010338