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gaze palsy, familial horizontal, with progressive scoliosis 1

Disease Summary
Associated Targets (1)
Tbio

1


Uniprot Description An autosomal recessive neurologic disorder characterized by eye movement abnormalities apparent from birth, childhood-onset progressive scoliosis, distinctive brainstem malformation and defective crossing of some brainstem neuronal pathways.
Mondo Term and Equivalent IDs
MONDO:0020790:  gaze palsy, familial horizontal, with progressive scoliosis 1