intellectual disability, X-linked 97
Go to external page http://purl.obolibrary.org/obo/MONDO_0010430
Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the ZNF711 gene. [ MONDO:patterns/disease_series_by_gene ]
Synonyms: intellectual disability, X-linked 97 ZNF711 non-syndromic X-linked intellectual disability intellectual developmental disorder, X-linked 97 mental retardation, X-linked type 97 non-syndromic X-linked intellectual disability caused by mutation in ZNF711 intellectual disability, X-linked type 97
Term information
- UMLS:C2749020 (MONDO:equivalentTo)
- MESH:C567583 (MONDO:equivalentTo)
- MEDGEN:440689 (MONDO:equivalentTo)
- GARD:22686 (MONDO:GARD)
- DOID:0112046 (MONDO:equivalentTo)
- OMIM:300803 (MONDO:equivalentTo)
matrix_llm__is_cancer_other, gard_rare, matrix_llm__is_glucose_dysfunction_other, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, matrix_llm__txgnn_other, mondo_top_grouping_member, mondo_top_grouping_hereditary_disease, harrisons_view_psychiatric_disorder, matrix_included, nord_rare, matrix_llm__tag_existing_treatment_other, mondo_top_grouping_psychiatric_disorder, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, matrix_txgnn_grouping_member, rare, harrisons_view_member, mondo_top_grouping_nervous_system_disorder, matrix_txgnn_grouping_psychiatric_disorder, harrisons_view_hereditary_disease, harrisons_view_nervous_system_disorder
http://identifiers.org/mesh/C567583
http://purl.obolibrary.org/obo/DOID_0112046
http://identifiers.org/medgen/440689
https://omim.org/entry/300803
http://linkedlifedata.com/resource/umls/id/C2749020
intellectual disability, X-linked 65
MRX97
Mrxz
mental retardation, X-linked 65
mental retardation, X-linked 97
Term relations
- non-syndromic X-linked intellectual disability and has material basis in germline mutation in some ZNF711