[X] inherited lipid metabolism disorder
Go to external page http://purl.obolibrary.org/obo/MONDO_0002525
An inherited metabolic disorder caused by an enzyme deficiency, resulting in an inability to oxidize fatty acids for energy production. [ NCIT:C97092 ]
Term information
- NCIT:C97092 (MONDO:equivalentTo)
- Orphanet:309005 (MONDO:equivalentTo)
- MedDRA:10061227 (Orphanet:309005/e)
- UMLS:C0154251 (MONDO:equivalentTo)
- DOID:3146 (MONDO:equivalentTo)
- MEDGEN:57587 (MONDO:equivalentTo)
- ICD9:272.8 (MONDO:relatedTo)
- SCTID:267431006 (MONDO:equivalentTo)
- GARD:21314 (MONDO:GARD)
- ICD9:272.9 (MONDO:i2s)
- SCTID:402788005 (https://orcid.org/0009-0002-1597-2198)
gard_rare, matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, otar, matrix_excluded, disease_grouping, matrix_llm__tag_qualy_lost_other, matrix_llm__txgnn_other, matrix_llm__medical_specialization_other, mondo_top_grouping_member, 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://linkedlifedata.com/resource/umls/id/C0154251
http://identifiers.org/medgen/57587
http://purl.obolibrary.org/obo/DOID_3146
http://identifiers.org/snomedct/402788005
http://www.orpha.net/ORDO/Orphanet_309005
http://purl.obolibrary.org/obo/NCIT_C97092
http://identifiers.org/snomedct/267431006