PMC:5097349 / 11669-12555 JSONTXT

{"project":"AxD_symptoms","denotations":[{"id":"T53","span":{"begin":88,"end":94},"obj":"Phenotype"},{"id":"T54","span":{"begin":140,"end":167},"obj":"Phenotype"},{"id":"T55","span":{"begin":306,"end":320},"obj":"Phenotype"},{"id":"T56","span":{"begin":410,"end":429},"obj":"Phenotype"},{"id":"T57","span":{"begin":434,"end":453},"obj":"Phenotype"},{"id":"T58","span":{"begin":484,"end":502},"obj":"Phenotype"},{"id":"T59","span":{"begin":564,"end":581},"obj":"Phenotype"},{"id":"T60","span":{"begin":644,"end":667},"obj":"Phenotype"},{"id":"T61","span":{"begin":695,"end":712},"obj":"Phenotype"},{"id":"T62","span":{"begin":718,"end":744},"obj":"Phenotype"},{"id":"T63","span":{"begin":751,"end":775},"obj":"Phenotype"},{"id":"T64","span":{"begin":776,"end":790},"obj":"Phenotype"}],"attributes":[{"id":"A53","pred":"hp_id","subj":"T53","obj":"http://purl.obolibrary.org/obo/HP_0001251"},{"id":"A63","pred":"hp_id","subj":"T63","obj":"http://purl.obolibrary.org/obo/HP_0011096"},{"id":"A64","pred":"hp_id","subj":"T64","obj":"http://purl.obolibrary.org/obo/HP_0001271"},{"id":"A56","pred":"hp_id","subj":"T56","obj":"http://purl.obolibrary.org/obo/HP_0002352"},{"id":"A54","pred":"hp_id","subj":"T54","obj":"http://purl.obolibrary.org/obo/HP_0006994"},{"id":"A62","pred":"hp_id","subj":"T62","obj":"http://purl.obolibrary.org/obo/HP_0002326"},{"id":"A61","pred":"hp_id","subj":"T61","obj":"http://purl.obolibrary.org/obo/HP_0001251"},{"id":"A57","pred":"hp_id","subj":"T57","obj":"http://purl.obolibrary.org/obo/HP_0002313"},{"id":"A55","pred":"hp_id","subj":"T55","obj":"http://purl.obolibrary.org/obo/HP_0002415"},{"id":"A59","pred":"hp_id","subj":"T59","obj":"http://purl.obolibrary.org/obo/HP_0001268"},{"id":"A58","pred":"hp_id","subj":"T58","obj":"http://purl.obolibrary.org/obo/HP_0007024"},{"id":"A60","pred":"hp_id","subj":"T60","obj":"http://purl.obolibrary.org/obo/HP_0001278"}],"text":"X-ALD X-linked adrenoleukodystrophy, VWM Vanishing white matter disease, CACH childhood ataxia with central hypomylination, HDLS hereditary diffuse leukoencephalopathy with neuroaxonal spheroids, POLD Autosomal dominant pigmentary type of orthochromatic leucodystrophy, ADLD Adult-onset autosomal dominant leukodystrophy, NHD Nasu-Hakola disease, PLOSL polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy, SP spastic paraparesis, PP psychiatric problems, PBP pseudobulbar palsy, WM white matter, CWM cerebellar WM, PT pyramidal tracts, CD cognitive decline, AS autonomic symptoms, BBD bowel and bladder dysfunction, OH orthostatic hypotension, PS pyramidal symptoms, CA cerebellar ataxia, TIA transient ischemic attacks, PDPN peripheral demyelinating polyneuropathy, CST corticospinal tracts, CC corpus callosum, PWM periventricular WM, CP cerebellar peduncles\n"}