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
autosomal recessive kufs disease D009472
spielmeyer disease, vogt D009472
ceroid lipofuscinosis, neuronal D009472
ceroid-lipofuscinosis, CLN3-Related neuronal D009472
ceroid lipofuscinosis, neuronal 3, juvenile D009472
ceroid lipofuscinosis, neuronal 4 D009472
CLN3 related neuronal ceroid lipofuscinosis D009472
adult type neuronal ceroid lipofuscinosis D009472
kufs type neuronal ceroid lipofuscinosis D009472
ceroid lipofuscinosis, neuronal, 4a, autosomal recessive D009472
ceroid lipofuscinosis, neuronal, 4b, autosomal dominant D009472
disease, ceroid storage D009472
disease, lipofuscin storage D009472
storage disease, lipofuscin D009472
neuronal ceroid lipofuscinoses D009472