Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Laryngeal Diseases	[NCBI]

Gene	Link	Information Gain
GER	[NCBI]	0.00190747
CD68	[NCBI]	1.97133e-05
LAMB3	[NCBI]	1.59751e-05
EYA1	[NCBI]	9.87506e-06
KRT5	[NCBI]	8.72081e-06
KRT14	[NCBI]	8.39593e-06
SPP1	[NCBI]	8.13281e-06
EGFR	[NCBI]	8.10845e-06
CREBBP	[NCBI]	7.55162e-06
CD44	[NCBI]	7.48364e-06
TP63	[NCBI]	6.59584e-06
MMP9	[NCBI]	6.16588e-06
FASLG	[NCBI]	3.80897e-06
PCNA	[NCBI]	3.51758e-06
TNF	[NCBI]	1.75645e-06

OMIM	Link	Information gain
DIP	[NCBI]	0.000900049
hypertelorism with esophageal abnormality and hypospadias	[NCBI]	0.00059777
laryngomalacia	[NCBI]	0.000277646
alopecia universalis congenita, xy gonadal dysgenesis, and laryngomalacia	[NCBI]	0.000138346
laryngeal web, familial	[NCBI]	0.000115876
LOCS	[NCBI]	0.000101892
epidermolysis bullosa herpetiformis, dowling-meara type	[NCBI]	8.74777e-05
PC1	[NCBI]	7.99881e-05
lipoid proteinosis of urbach and wiethe	[NCBI]	7.03584e-05
KRT14	[NCBI]	5.90902e-05
KRT5	[NCBI]	5.79854e-05
TNC	[NCBI]	4.61971e-05
EGFR	[NCBI]	3.78169e-05
HD	[NCBI]	2.70459e-05
SLE	[NCBI]	2.62883e-05
PCNA	[NCBI]	1.38818e-05
RA	[NCBI]	1.35154e-05
MG	[NCBI]	7.88196e-06
TNF	[NCBI]	5.89603e-06