Mondo_2019_Kim Find_IDs Find_Terms Annotation
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created at 2021-12-20 07:01:32 UTC
updated at 2021-12-22 01:40:39 UTC
Mondo_2019_Kim from bioportal
113,078 entries

There is 0 pattern entry.

Label
Id
ARCL3A http://purl.obolibrary.org/obo/MONDO_0009053
P5CS deficiency http://purl.obolibrary.org/obo/MONDO_0009053
ALDH18A1-related de Barsy syndrome http://purl.obolibrary.org/obo/MONDO_0009053
neurocutaneous syndrome, Bicknell type http://purl.obolibrary.org/obo/MONDO_0009053
cutis laxa, autosomal recessive, type 3A http://purl.obolibrary.org/obo/MONDO_0009053
cutis laxa, autosomal recessive, type IIIA http://purl.obolibrary.org/obo/MONDO_0009053
cutis laxa, autosomal recessive, type IIIA; ARCL3A http://purl.obolibrary.org/obo/MONDO_0009053
cutis laxa, corneal clouding, and mental retardation http://purl.obolibrary.org/obo/MONDO_0009053
autosomal recessive cutis laxa type IIIA http://purl.obolibrary.org/obo/MONDO_0009053
progeroid syndrome of De Barsy http://purl.obolibrary.org/obo/MONDO_0009053
De Barsy syndrome A http://purl.obolibrary.org/obo/MONDO_0009053
De Barsy syndrome a http://purl.obolibrary.org/obo/MONDO_0009053
Delta-1-pyrroline 5-carboxylate synthetase deficiency http://purl.obolibrary.org/obo/MONDO_0009053
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