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
CLN4B 8083
CLN4B disease 8083
adult neuronal ceroid lipofuscinosis 4B 8083
noonan syndrome 5 C548083
autosomal dominant Kufs disease 8083
Kuf's disease, autosomal dominant 8083
Kufs disease, autosomal dominant 8083
duplication 1q32 qter C538083
tyrosine-oxidase temporary deficiency 18083
neuronal ceroid lipofuscinosis 4 parry type 8083
neuronal ceroid lipofuscinosis 4B 8083
neuronal ceroid lipofuscinosis type 4B 8083
neuronal ceroid lipofuscinosis, parry type 8083
autosomal dominant neuronal ceroid lipofuscinosis 4B 8083
ceroid lipofuscinosis, neuronal, 4B, autosomal dominant 8083