MONDO_merge Find_IDs Find_Terms Annotation
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created at 2021-12-22 03:08:20 UTC
updated at 2021-12-22 07:06:09 UTC
MONDO_bioport_pref_name
183,974 entries
Label
Id
AD-SPG9A 11006
SPG9A 11006
cataracts with motor neuronopathy, short stature and skeletal abnormalities 11006
spastic paraplegia 9A, autosomal dominant 11006
spastic paraplegia 9A, autosomal dominant; SPG9A http://purl.obolibrary.org/obo/MONDO_0011006
intestinalis, pneumatosis cystoides D011006
autosomal dominant complex spastic paraplegia type 9A 11006
cataracts with motor neuronopathy, short stature, and skeletal abnormalities 11006
cystoides intestinalis, pneumatosis D011006
cataracts motor neuropathy-short stature-skeletal anomalies syndrome 11006
hereditary spastic paraplegia 9A 11006
hereditary spastic paraplegia type 9A 11006
spastic paraparesis with amyopathy, cataracts and gastroesophageal reflux 11006
autosomal dominant spastic paraplegia 9A 11006
spastic paraparesis with amyopathy, cataracts, and gastroesophageal reflux 11006