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