Lhermitte-Duclos disease (LDD) is a very rare disorder characterized by abnormal development and enlargement of the cerebellum, and an increased intracranial pressure. [ Orphanet:65285 ]
Synonyms: dysplastic gangliocytoma of cerebellum dysplastic cerebellar gangliocytoma dysplastic gangliocytoma of the cerebellum LDD
Term information
- MEDGEN:140251 (MONDO:equivalentTo)
- NCIT:C8419 (MONDO:equivalentTo)
- Orphanet:65285 (MONDO:equivalentTo)
- UMLS:C0391826 (MONDO:equivalentTo)
- ICDO:9493/0 (NCIT:C8419)
- GARD:6901 (MONDO:GARD)
ordo_disorder, matrix_llm__is_cancer_other, gard_rare, matrix_txgnn_grouping_cancer_or_benign_tumor, matrix_llm__txgnn_other, mondo_top_grouping_member, matrix_included, nord_rare, mondo_top_grouping_cancer_or_benign_tumor, matrix_txgnn_grouping_member, rare, orphanet_rare, harrisons_view_nervous_system_disorder, matrix_llm__is_glucose_dysfunction_other, otar, harrisons_view_disorder_of_development_or_morphogenesis, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, matrix_llm__tag_existing_treatment_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_cancer_or_benign_tumor, harrisons_view_member, mondo_top_grouping_nervous_system_disorder, mondo_top_grouping_disorder_of_development_or_morphogenesis
http://purl.obolibrary.org/obo/NCIT_C8419
http://identifiers.org/medgen/140251
http://www.orpha.net/ORDO/Orphanet_65285
http://linkedlifedata.com/resource/umls/id/C0391826