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MeSH keywords -> Related genes, diseases (OMIM)


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01 Nail-Patella Syndrome [NCBI]


Gene


Gene Link Information
Gain
01
PTLAH [NCBI] 0.000499621
LMX1B [NCBI] 0.000401759
LDB1 [NCBI] 2.48331e-05
ABO [NCBI] 2.22436e-05
COL5A1 [NCBI] 1.08556e-05
EXT1 [NCBI] 9.6885e-06
PAX2 [NCBI] 7.71974e-06
NOG [NCBI] 7.43522e-06
NPHS1 [NCBI] 6.37926e-06
MEFV [NCBI] 6.00309e-06
FGFR3 [NCBI] 5.35143e-06




OMIM


OMIM Link Information
gain
01
NPS [NCBI] 0.0079001
PTLAH [NCBI] 0.00098052
radial heads, posterior dislocation of [NCBI] 0.00098052
LMX1B [NCBI] 0.000971728
koilonychia, hereditary [NCBI] 0.000844965
deafness, congenital, and onychodystrophy, recessive form [NCBI] 0.000632907
alport syndrome, autosomal dominant [NCBI] 0.000450974
AK1 [NCBI] 0.000183798
ABO [NCBI] 0.000124512
COL5A1 [NCBI] 0.000124512
nail-patella-like renal disease [NCBI] 0.000116948
GLC1A [NCBI] 0.000107551
POAG [NCBI] 0.000107551
ASS [NCBI] 8.97759e-05
TBX4 [NCBI] 7.59186e-05
SPS [NCBI] 7.31844e-05
ehlers-danlos syndrome, type ii [NCBI] 6.12812e-05
HHT [NCBI] 2.86036e-05
BCNS [NCBI] 1.94512e-05
FMF [NCBI] 3.75183e-06




Database Center for Life Science