ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome
Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome is a rare neuro-ophthalmological disease characterized by nonprogressive cerebellar ataxia, delayed motor and language development, and intellectual disability in addition to ophthalmological abnormalities (e.g. oculomotor apraxia, strabismus, amblyopia, retinal dystrophy, and myopia). Cerebellar cysts, cerebellar dysplasia and cerebellar vermis hypoplasia, seen on magnetic resonance imaging, are also characteristic of the disease. [ Orphanet:370022 ]
Term info
- UMLS:C4014821 (MONDO:ncbi_mim2gene_medline)
- OMIM:615960 (Orphanet:370022/e)
- Orphanet:370022 (OMIM:615960)
ordo_disease
https://github.com/monarch-initiative/mondo/issues/5588
Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome is a rare neuro-ophthalmological disease characterized by nonprogressive cerebellar ataxia, delayed motor and language development, and intellectual disability in addition to ophthalmological abnormalities (e.g. oculomotor apraxia, strabismus, amblyopia, retinal dystrophy, and myopia). Cerebellar cysts, cerebellar dysplasia and cerebellar vermis hypoplasia, seen on magnetic resonance imaging, are also characteristic of the disease.
http://purl.obolibrary.org/obo/Orphanet_370022, http://linkedlifedata.com/resource/umls/id/C4014821, https://omim.org/entry/615960
http://purl.obolibrary.org/obo/MONDO_0000508
ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome, Poretti-Boltshauser syndrome
PTBHS, PORETTI-Boltshauser syndrome
MONDO:0014419