TCMD15967 |
Myopathy, Centronuclear, 1 |
MalaCards;DisGeNET |
TCMD19471 |
Primary Progressive Aphasia (disorder) |
CTD;DisGeNET |
TCMD19577 |
Promyelocytic leukemia |
DisGeNET |
TCMD21743 |
Smith-Magenis syndrome |
CTD;MalaCards;DisGeNET |
TCMD23182 |
Thyroiditis |
CTD;DisGeNET |