DisGeNET - a database of gene-disease associations

RMND1, required for meiotic nuclear division 1 homolog, 55005

N. diseases: 59; N. variants: 15

Disease: hearing impairment ×

Source: ALL

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _g

DPI _g

pLI

EI _gda

EL _gda

Score _gda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Disease

Score _gda

Association Type

Type

Original DB

Sentence supporting the association

PMID

PMID Year

CUI:	C1384666
Disease:	hearing impairment

hearing impairment

0.110

GeneticVariation

phenotype

BEFREE

Hearing impairment and renal failure associated with RMND1 mutations.

2016

CUI:	C1384666
Disease:	hearing impairment

hearing impairment

0.110

Biomarker

phenotype

HPO