ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome
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ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome
Summary
ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome is a developmental defect during embryogenesis[1].
Key Facts
- ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome's instance of is recorded as developmental defect during embryogenesis[2].
- ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome's instance of is recorded as rare disease[3].
- ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome's instance of is recorded as class of disease[4].
- ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome is a type of rare genetic developmental defect during embryogenesis[5].
- ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome is a type of syndrome with a cerebellar malformation as major feature[6].
- ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome is a type of oculomotor apraxia[7].
- ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome is a type of genetic syndromic intellectual disability[8].
- ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome's genetic association is recorded as LAMA1[9].
- ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_370022[10].