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
AI2A1 8772
JBTS 18772
cerebelloparenchymal disorder IV 18772
CPD IV 18772
Joubert syndrome 18772
Joubert-Boltshauser syndrome 18772
amelogenesis imperfecta caused by mutation in KLK4 8772
cerebellar vermis agenesis 18772
KLK4 amelogenesis imperfecta 8772
amelogenesis imperfecta, hypomaturation type, IIA1 8772
amelogenesis imperfecta, hypomaturation type, IIA1; AI2A1 http://purl.obolibrary.org/obo/MONDO_0008772
amelogenesis imperfecta pigmented hypomaturation type 8772
amelogenesis imperfecta pigmented hypomaturation type 1 8772
amelogenesis imperfecta, pigmented hypomaturation type, 1 8772
Joubert syndrome type A 18772