|
thin-basement-membrane nephropathy
|
7709 |
|
|
hermansky-pudlak syndrome 2
|
C537709 |
|
|
platelet defects and oculocutaneous albinism
|
C537709 |
|
|
muscular dystrophy, congenital, due to integrin alpha-7 deficiency
|
C567709 |
|
|
myopathy, congenital, due to integrin alpha-7 deficiency
|
C567709 |
|
|
hematuria, benign familial
|
7709 |
|
|
hematuria, benign familial; BFH
|
http://purl.obolibrary.org/obo/MONDO_0007709 |
|
|
disorder of lipid absorption and transport
|
17709 |
|
|
thin membrane nephropathy
|
7709 |
|
|
hermansky pudlak syndrome 2
|
C537709 |
|
|
congenital, due to integrin alpha-7 deficiency muscular dystrophy
|
C567709 |
|
|
congenital, due to integrin alpha-7 deficiency myopathy
|
C567709 |
|
