RHBDF2, rhomboid 5 homolog 2, 79651

N. diseases: 90; N. variants: 5
Disease: Keratosis Palmaris et Plantaris Familiaris ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3489771
Disease: Keratosis Palmaris et Plantaris Familiaris
Keratosis Palmaris et Plantaris Familiaris 		0.200 Biomarker disease MGD Genetic deletion of amphiregulin restores the normal skin phenotype in a mouse model of the human skin disease tylosis. 28655741 2017
CUI: C3489771
Disease: Keratosis Palmaris et Plantaris Familiaris
Keratosis Palmaris et Plantaris Familiaris 		0.200 Biomarker disease MGD Tissue-specific role of RHBDF2 in cutaneous wound healing and hyperproliferative skin disease. 29116018 2017
CUI: C3489771
Disease: Keratosis Palmaris et Plantaris Familiaris
Keratosis Palmaris et Plantaris Familiaris 		0.200 Biomarker disease MGD Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5. 12573256 2003