[X] disorder of protein O-glycosylation
Go to external page http://purl.obolibrary.org/obo/MONDO_0017741
A disease that has its basis in the disruption of protein O-linked glycosylation. [ MONDO:patterns/basis_in_disruption_of_process ]
Synonyms: disorder of protein O-linked glycosylation protein O-linked glycosylation disease
Term information
- UMLS:C5681041 (MONDO:equivalentTo)
- Orphanet:309447 (MONDO:equivalentTo)
- icd11.foundation:1883085871 (https://orcid.org/0000-0002-4142-7153)
- GARD:21336 (MONDO:GARD)
- MEDGEN:1842631 (MONDO:equivalentTo)
matrix_llm__is_cancer_other, gard_rare, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, matrix_llm__tag_qualy_lost_other, disease_grouping, mondo_top_grouping_member, matrix_llm__txgnn_other, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, matrix_llm__tag_existing_treatment_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, mondo_top_grouping_metabolic_disease, matrix_txgnn_grouping_metabolic_disease, matrix_txgnn_grouping_member, rare, harrisons_view_member, harrisons_view_hereditary_disease, ordo_group_of_disorders, harrisons_view_metabolic_disease
http://purl.obolibrary.org/obo/mondo/patterns/basis_in_disruption_of_process.yaml
http://purl.obolibrary.org/obo/mondo/patterns/disrupts_process.yaml
http://identifiers.org/medgen/1842631
http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1883085871
http://linkedlifedata.com/resource/umls/id/C5681041
http://www.orpha.net/ORDO/Orphanet_309447