PubDictionaries

MONDO (121,242) Find_IDs Annotation

manager	jdkim
language	-
license	-
created at	2019-07-11 18:15:35 UTC
updated at	2020-12-23 10:47:34 UTC

diseases or disorders as defined in MONDO disease ontology (the version released on 2019-05-28). The terms are sourced from BioPortal on July 12, 2019.

There is 0 pattern entry.

Label	Id

spinocerebellar ataxia type 18	http://purl.obolibrary.org/obo/MONDO_0011834
sensorimotor neuropathy with ataxia autosomal dominant	http://purl.obolibrary.org/obo/MONDO_0011834
spinocerebellar ataxia 18; SCA18	http://purl.obolibrary.org/obo/MONDO_0011834
SMNA	http://purl.obolibrary.org/obo/MONDO_0011834
SCA18	http://purl.obolibrary.org/obo/MONDO_0011834
sensorimotor neuropathy with ataxia, autosomal dominant	http://purl.obolibrary.org/obo/MONDO_0011834
spinocerebellar ataxia 18	http://purl.obolibrary.org/obo/MONDO_0011834
sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome	http://purl.obolibrary.org/obo/MONDO_0011835
SANDO	http://purl.obolibrary.org/obo/MONDO_0011835
spinocerebellar ataxia with epilepsy	http://purl.obolibrary.org/obo/MONDO_0011835
epilepsy, progressive myoclonic, with sensory ataxic neuropathy	http://purl.obolibrary.org/obo/MONDO_0011835
sensory ataxic neuropathy, dysarthria, and ophthalmoparesis	http://purl.obolibrary.org/obo/MONDO_0011835
epilepsy, progressive myoclonic, 5, formerly	http://purl.obolibrary.org/obo/MONDO_0011835
sensory ataxic neuropathy, dysarthria, and ophthalmoparesis; SANDO	http://purl.obolibrary.org/obo/MONDO_0011835
sensory ataxic neuropathy with mitochondrial DNA deletions, autosomal recessive	http://purl.obolibrary.org/obo/MONDO_0011835