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Dowling-Degos disease 1

Go to external page http://purl.obolibrary.org/obo/MONDO_0024534

Any Dowling-Degos disease in which the cause of the disease is a mutation in the KRT5 gene. [ MONDO:patterns/disease_series_by_gene ]

Synonyms: KRT5 Dowling-Degos disease Dowling-Degos disease 1 Dowling-Degos disease caused by mutation in KRT5

This is just here as a test because I lose it

Term information

database cross reference
Subsets

matrix_llm__is_cancer_other, gard_rare, matrix_llm__is_glucose_dysfunction_other, mondo_top_grouping_integumentary_system_disorder, matrix_llm__tag_qualy_lost_other, mondo_top_grouping_member, matrix_llm__medical_specialization_other, matrix_llm__txgnn_other, mondo_top_grouping_hereditary_disease, nord_rare, matrix_included, matrix_llm__tag_existing_treatment_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, mondo_top_grouping_metabolic_disease, matrix_txgnn_grouping_metabolic_disease, matrix_txgnn_grouping_member, rare, harrisons_view_member, harrisons_view_hereditary_disease, harrisons_view_integumentary_system_disorder, harrisons_view_metabolic_disease

exactMatch

http://linkedlifedata.com/resource/umls/id/C4552092

https://omim.org/entry/179850

http://identifiers.org/medgen/1645697

has related synonym

DDD1

DDD

reticular pigment anomaly of flexures

id

MONDO:0024534