congenital reticular ichthyosiform erythroderma
Go to external page http://purl.obolibrary.org/obo/MONDO_0012208
Synonyms: IWC CRIE ichthyosis variegata ichthyosis with confetti
Term information
- GARD:17305 (MONDO:GARD)
- OMIM:609165 (Orphanet:281190/e)
- MESH:C563781 (MONDO:equivalentTo)
- UMLS:C3665704 (MONDO:equivalentTo)
- Orphanet:281190 (OMIM:609165)
- MEDGEN:777141 (MONDO:equivalentTo)
- icd11.foundation:565254051 (MONDO:equivalentTo)
- SCTID:703504006 (MONDO:equivalentTo)
matrix_llm__is_cancer_other, ordo_disorder, gard_rare, matrix_llm__is_glucose_dysfunction_other, otar, 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, mondo_top_grouping_hereditary_disease, matrix_included, matrix_llm__tag_existing_treatment_other, nord_rare, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, rare, harrisons_view_member, harrisons_view_hereditary_disease, orphanet_rare, harrisons_view_integumentary_system_disorder
http://identifiers.org/medgen/777141
http://www.orpha.net/ORDO/Orphanet_281190
https://omim.org/entry/609165
http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/565254051
http://identifiers.org/snomedct/703504006
http://identifiers.org/mesh/C563781
http://linkedlifedata.com/resource/umls/id/C3665704
erythroderma, ichthyosiform, congenital reticular
erythrokeratoderma, reticular
Aarau disease
https://github.com/monarch-initiative/mondo/issues/6749
https://github.com/monarch-initiative/mondo/issues/6877
https://github.com/monarch-initiative/mondo/issues/4069
Term relations
- [X] keratinopathic ichthyosis
- has characteristic some congenital
- has material basis in germline mutation in some KRT10