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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
SPG9 15091
autosomal dominant spastic paraplegia type 9 15091
autosomal dominant complex spastic paraplegia caused by mutation in ALDH18A1 15091
bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophy 15091
spastic paraplegia 9 15091
ALDH18A1 autosomal dominant complex spastic paraplegia 15091
cataracts, motor neuronopathy, short stature and skeletal abnormalities 15091
spastic paraparesis-amyopathy-cataracts-gastroesophageal reflux syndrome 15091
cataracts-motor neuropathy-short stature-skeletal anomalies syndrome 15091
autosomal dominant spastic paraparesis 15091