A pigmentation disease characterized by a reticulate pattern of abnormally dark skin coloring, particularly in the body's folds and creases. [ http://ghr.nlm.nih.gov/condition/dowling-degos-disease http://en.wikipedia.org/wiki/Reticular_pigmented_anomaly_of_the_flexures DOID:0060256 ]
Synonyms: Dowling-Degos disease type 1 dark dot disease reticular pigment anomaly of flexures
Term information
- Orphanet:79145 (OMIM:179850)
- DOID:0060256 (MONDO:equivalentTo)
- UMLS:C3714534 (MONDO:equivalentTo)
- MESH:C562924 (MONDO:equivalentTo)
- MEDGEN:811363 (MONDO:equivalentTo)
- SCTID:239133004 (MONDO:directSiblingOf)
- icd11.foundation:15123132 (MONDO:equivalentTo)
- GARD:9775 (MONDO:GARD)
- MedDRA:10068651 (Orphanet:79145/e)
matrix_llm__is_cancer_other, ordo_disorder, gard_rare, mondo_top_grouping_integumentary_system_disorder, matrix_llm__txgnn_other, mondo_top_grouping_member, nord_rare, matrix_included, mondo_top_grouping_metabolic_disease, matrix_txgnn_grouping_member, rare, orphanet_rare, harrisons_view_integumentary_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, matrix_llm__tag_existing_treatment_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, matrix_txgnn_grouping_metabolic_disease, harrisons_view_member, harrisons_view_hereditary_disease, harrisons_view_metabolic_disease
http://identifiers.org/mesh/C562924
http://purl.obolibrary.org/obo/DOID_0060256
http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/15123132
http://linkedlifedata.com/resource/umls/id/C3714534
http://identifiers.org/medgen/811363
http://www.orpha.net/ORDO/Orphanet_79145