Disease: Alopecia universalis congenita ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1859877
Disease: Alopecia universalis congenita
Alopecia universalis congenita 		0.900 GeneticVariation disease UNIPROT Hairless is a histone H3K9 demethylase. 24334705 2014
CUI: C1859877
Disease: Alopecia universalis congenita
Alopecia universalis congenita 		0.900 Biomarker disease MGD A novel nonsense mutation and polymorphisms in the mouse hairless gene. 15955095 2005
CUI: C1859877
Disease: Alopecia universalis congenita
Alopecia universalis congenita 		0.900 GeneticVariation disease UNIPROT A novel missense mutation affecting the human hairless thyroid receptor interacting domain 2 causes congenital atrichia. 12406339 2002
CUI: C1859877
Disease: Alopecia universalis congenita
Alopecia universalis congenita 		0.900 Biomarker disease MGD Molecular basis for the rhino (hrrh-8J) phenotype: a nonsense mutation in the mouse hairless gene. 9799606 1998
CUI: C1859877
Disease: Alopecia universalis congenita
Alopecia universalis congenita 		0.900 GeneticVariation disease UNIPROT Alopecia universalis associated with a mutation in the human hairless gene. 9445480 1998
CUI: C1859877
Disease: Alopecia universalis congenita
Alopecia universalis congenita 		0.900 Biomarker disease MGD Molecular basis of a novel rhino (hr(rhChr)) phenotype: a nonsense mutation in the mouse hairless gene. 9832318 1998
CUI: C1859877
Disease: Alopecia universalis congenita
Alopecia universalis congenita 		0.900 CausalMutation disease CLINVAR Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia. 9736769 1998
CUI: C1859877
Disease: Alopecia universalis congenita
Alopecia universalis congenita 		0.900 GeneticVariation disease UNIPROT Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia. 9736769 1998
CUI: C1859877
Disease: Alopecia universalis congenita
Alopecia universalis congenita 		0.900 Biomarker disease CTD_human
CUI: C1859877
Disease: Alopecia universalis congenita
Alopecia universalis congenita 		0.900 Biomarker disease GENOMICS_ENGLAND