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[X] inherited epidermolysis bullosa

Go to external page http://purl.obolibrary.org/obo/MONDO_0019276

Inherited epidermolysis bullosa (EB) encompasses a number of disorders characterized by recurrent blister formation as the result of structural fragility within the skin and selected other tissues. [ Orphanet:79361 ]

Synonyms: epidermolysis bullosa hereditaria hereditary epidermolysis bullosa

This is just here as a test because I lose it

Term information

database cross reference
  • MEDGEN:697573 (MONDO:equivalentTo)
  • UMLS:C1274224 (MONDO:equivalentTo)
  • SCTID:402781004 (MONDO:equivalentTo)
  • ICD9:757.39 (MONDO:relatedTo)
  • Orphanet:79361 (MONDO:equivalentTo)
  • GARD:18992 (MONDO:GARD)
Subsets

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

exactMatch

http://linkedlifedata.com/resource/umls/id/C1274224

http://identifiers.org/snomedct/402781004

http://www.orpha.net/ORDO/Orphanet_79361

http://identifiers.org/medgen/697573

id

MONDO:0019276