spastic paraplegia 88, autosomal dominant
Go to external page http://purl.obolibrary.org/obo/MONDO_0859309
Term information
- MEDGEN:1824020 (MONDO:equivalentTo)
- UMLS:C5774247 (MONDO:equivalentTo)
- DOID:0070457 (MONDO:equivalentTo)
- OMIM:620106 (MONDO:equivalentTo)
gard_rare, matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, 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_txgnn_grouping_neurodegenerative_disease, matrix_llm__tag_existing_treatment_other, matrix_included, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, matrix_txgnn_grouping_member, rare, harrisons_view_member, mondo_top_grouping_nervous_system_disorder, harrisons_view_hereditary_disease, harrisons_view_nervous_system_disorder
https://omim.org/entry/620106
http://linkedlifedata.com/resource/umls/id/C5774247
http://identifiers.org/medgen/1824020
http://purl.obolibrary.org/obo/DOID_0070457