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[X] erythrokeratoderma

Go to external page http://purl.obolibrary.org/obo/MONDO_0019270

An umbrella term for a group of rare genetic skin disorders characterized by well-demarcated plaques of reddened, dry and thickened skin. Typically, these lesions are distributed symmetrically on the body and tend to slowly expand and progress over time. [ https://rarediseases.org/rare-diseases/https-rarediseases-org-rare-diseases-erythrokeratoderma/ https://orcid.org/0000-0001-5208-3432 ]

This is just here as a test because I lose it

Term information

database cross reference
  • MEDGEN:609461 (MONDO:equivalentTo)
  • GARD:18986 (MONDO:GARD)
  • SCTID:254215005 (MONDO:equivalentTo)
  • MedDRA:10015280 (Orphanet:79355/e)
  • ICD9:757.39 (MONDO:relatedTo)
  • Orphanet:79355 (MONDO:equivalentTo)
  • UMLS:C0432330 (MONDO:equivalentTo)
Subsets

gard_rare, matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, otar, matrix_llm__tag_qualy_lost_other, mondo_top_grouping_integumentary_system_disorder, disease_grouping, mondo_top_grouping_member, matrix_llm__medical_specialization_other, matrix_llm__txgnn_other, matrix_llm__tag_existing_treatment_other, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, rare, harrisons_view_member, ordo_group_of_disorders, harrisons_view_integumentary_system_disorder

closeMatch

http://identifiers.org/meddra/10015280

exactMatch

http://identifiers.org/medgen/609461

http://linkedlifedata.com/resource/umls/id/C0432330

http://www.orpha.net/ORDO/Orphanet_79355

http://identifiers.org/snomedct/254215005

id

MONDO:0019270

Term relations

Subclass of: