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[X] hereditary epidermal appendage anomaly

Go to external page http://purl.obolibrary.org/obo/MONDO_0021026

An instance of epidermal appendage anomaly that is caused by a modification of the individual's genome. [ MONDO:patterns/genetic ]

Synonyms: genetic epidermal appendage anomaly

This is just here as a test because I lose it

Term information

database cross reference
  • MEDGEN:1843118 (MONDO:equivalentTo)
  • Orphanet:183447 (MONDO:equivalentTo)
  • GARD:20265 (MONDO:GARD)
  • UMLS:C5680583 (MONDO:equivalentTo)
Subsets

matrix_llm__is_cancer_other, gard_rare, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, mondo_top_grouping_integumentary_system_disorder, matrix_llm__tag_qualy_lost_other, mondo_top_grouping_member, matrix_llm__txgnn_other, matrix_llm__medical_specialization_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, harrisons_view_integumentary_system_disorder, ordo_group_of_disorders

exactMatch

http://linkedlifedata.com/resource/umls/id/C5680583

http://www.orpha.net/ORDO/Orphanet_183447

http://identifiers.org/medgen/1843118

id

MONDO:0021026

Term relations

Subclass of: