An X-linked intellectual deficiency in which not enough information is known, reported or published to indicate whether a gene causes non-syndromic or syndromic presentations. [ https://clinicalgenome.org/affiliation/40006/ ]
Synonyms: X-linked intellectual disability
Term information
- MEDGEN:211749 (MONDO:equivalentTo)
- UMLS:C1136249 (MONDO:equivalentTo)
matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, otar, matrix_llm__tag_qualy_lost_other, mondo_top_grouping_member, matrix_llm__medical_specialization_other, matrix_llm__txgnn_other, mondo_top_grouping_hereditary_disease, harrisons_view_psychiatric_disorder, matrix_included, matrix_llm__tag_existing_treatment_other, clingen, mondo_top_grouping_psychiatric_disorder, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, matrix_txgnn_grouping_member, harrisons_view_member, mondo_top_grouping_nervous_system_disorder, harrisons_view_hereditary_disease, matrix_txgnn_grouping_psychiatric_disorder, harrisons_view_nervous_system_disorder