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non-syndromic X-linked intellectual disability

Go to external page http://purl.obolibrary.org/obo/MONDO_0019181

Nonspecific X-linked intellectual deficiencies (MRX) belong to the family of sex-linked intellectual deficiencies (XLMR). In contrast to syndromic or specific X-linked intellectual deficiencies (MRXS), which also present with associated physical, neurological and/or psychiatric manifestations, intellectual deficiency is the only symptom of MRX. [ Orphanet:777 ]

Synonyms: non-specific X-linked mental retardation intellectual disability, nonsyndromic, X-linked non-specific X-linked intellectual disability intellectual disability, X-linked, nonsyndromic X-linked non-specific intellectual disability mental retardation, X-linked, nonsyndromic X-linked non-syndromic intellectual disability non-syndromic intellectual disability, X-linked nonsyndromic X-linked intellectual disability non-syndromic X-linked intellectual disability mental retardation, nonsyndromic, X-linked

This is just here as a test because I lose it

Term information

database cross reference
  • Orphanet:777 (MONDO:equivalentTo)
  • MEDGEN:502019 (MONDO:equivalentTo)
  • GARD:18640 (MONDO:GARD)
  • MESH:C564490 (MONDO:equivalentTo)
  • DOID:0050776 (MONDO:equivalentTo)
  • UMLS:C3501611 (MONDO:equivalentTo)
  • OMIMPS:309530 (MONDO:equivalentTo)
Subsets

matrix_llm__is_cancer_other, gard_rare, matrix_llm__txgnn_other, mondo_top_grouping_member, harrisons_view_psychiatric_disorder, nord_rare, matrix_included, clingen, matrix_txgnn_grouping_member, rare, matrix_txgnn_grouping_psychiatric_disorder, harrisons_view_nervous_system_disorder, matrix_llm__is_glucose_dysfunction_other, otar, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, ordo_subtype_of_a_disorder, matrix_llm__tag_existing_treatment_other, ordo_etiological_subtype, mondo_top_grouping_psychiatric_disorder, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_member, mondo_top_grouping_nervous_system_disorder, harrisons_view_hereditary_disease

A synonym that is historic and discouraged
mental retardation, nonsyndromic, X-linked

ClinGen label
non-syndromic X-linked intellectual disability [ DOID:0050776 ]

A synonym that is historic and discouraged
mental retardation, X-linked, nonsyndromic [ MONDO:0000168 ]

A synonym that is historic and discouraged
non-specific X-linked mental retardation [ DOID:0050776 ]

curated content resource

https://search.clinicalgenome.org/kb/conditions/MONDO:0019181

exactMatch

https://omim.org/phenotypicSeries/PS309530

http://www.orpha.net/ORDO/Orphanet_777

http://purl.obolibrary.org/obo/DOID_0050776

http://identifiers.org/mesh/C564490

http://identifiers.org/medgen/502019

http://linkedlifedata.com/resource/umls/id/C3501611

has related synonym

isolated X-linked intellectual disability

id

MONDO:0019181

should conform to

http://purl.obolibrary.org/obo/mondo/patterns/OMIM_phenotypic_series.yaml