/infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome

infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome

Rare Disease

MONDO:0033864

Also Known As

Baker-Gordon syndrome

Comprehensive, easy-to-understand information about this condition

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Gene data from MyGene.info • Click to view on NCBI Gene

Neu-Laxova syndrome

MONDO:0000179

cerebellar ataxia

MONDO:0000437

inclusion body myopathy with Paget disease of bone and frontotemporal dementia

MONDO:0000507

syndromic intellectual disability

MONDO:0000508

abdominal obesity-metabolic syndrome

MONDO:0000816

fibrogenesis imperfecta ossium

MONDO:0000849