MONDO_merge Find_IDs Find_Terms Annotation
manager
language -
license -
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
NTEMND 12787
SPG39 12787
spastic paraplegia 39, autosomal recessive 12787
spastic paraplegia 39 12787
spastic paraplegia 39, autosomal recessive; SPG39 http://purl.obolibrary.org/obo/MONDO_0012787
NTE related motor neuron disorder 12787
autosomal recessive spastic paraplegia type 39 12787
spastic paraplegia due to NTE mutation 12787
spastic paraplegia due to neuropathy target esterase mutation 12787
NTE-related motor neuron disorder 12787
hereditary spastic paraplegia 39 12787
hereditary spastic paraplegia caused by mutation in PNPLA6 12787
hereditary spastic paraplegia type 39 12787
PNPLA6 hereditary spastic paraplegia 12787
autosomal recessive spastic paraplegia 39 12787