Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Pediatrics [NCBI]

Gene


 Gene Link Information
Gain		 01



OMIM


 OMIM Link Information
gain		 01
apnea, obstructive sleep [NCBI] 0.000835316
VUR1 [NCBI] 0.000710915
CF [NCBI] 0.000268936
amyotonia congenita [NCBI] 0.000152565
thrombocytopenic purpura, autoimmune [NCBI] 0.000113753
rheumatoid arthritis, systemic juvenile [NCBI] 9.22454e-05
mucopolysaccharidosis type iva [NCBI] 8.00602e-05
EBN1 [NCBI] 7.42516e-05
glycogen storage disease iii [NCBI] 7.03681e-05
thrombasthenia of glanzmann and naegeli [NCBI] 4.61245e-05
CDLS1 [NCBI] 4.2726e-05
KCNQ2 [NCBI] 4.13781e-05
CJD [NCBI] 3.27593e-05
HPRT1 [NCBI] 2.90912e-05
SLE [NCBI] 2.84457e-05
MODY [NCBI] 2.69822e-05
GJB2 [NCBI] 2.64416e-05
MFS [NCBI] 2.64101e-05
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency [NCBI] 2.62588e-05
RTT [NCBI] 2.49541e-05
GTS [NCBI] 2.05391e-05
FA [NCBI] 1.11585e-05



Database Center for Life Science