Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Hemoglobin H [NCBI]

Gene


 Gene Link Information
Gain		 01
HBAP1 [NCBI] 0.000218098
HBA2 [NCBI] 1.66351e-05
HBA1 [NCBI] 1.52084e-05
HBB [NCBI] 3.43587e-06
HBZ [NCBI] 2.29668e-06
G6PD [NCBI] 1.23308e-06
EPO [NCBI] 9.39729e-07



OMIM


 OMIM Link Information
gain		 01
ATRX [NCBI] 0.00128274
alpha-thalassemia/mental retardation syndrome, deletion-type [NCBI] 0.00027668
HBA2 [NCBI] 0.000204758
HBA1 [NCBI] 0.000170456
ATMDS [NCBI] 0.000150884
MRXHF1 [NCBI] 0.000114103
hemoglobin--variants for which the chain carrying the mutation is unknown or uncertain [NCBI] 0.000101779
HBB [NCBI] 8.38082e-05
ATRX [NCBI] 5.75633e-05
polycystic kidneys [NCBI] 4.63859e-05
HBZ [NCBI] 2.8801e-05
G6PD [NCBI] 6.79861e-06
EPO [NCBI] 2.56129e-06
VEGF [NCBI] 1.41797e-08



Database Center for Life Science