|
lymphedema, hereditary, IC; LMPH1C
|
http://purl.obolibrary.org/obo/MONDO_0013278 |
|
|
ischiocoxopodopatellar syndrome; ICPPS
|
http://purl.obolibrary.org/obo/MONDO_0007841 |
|
|
lattice type II corneal dystrophy
|
C000657784 |
|
|
groenouw type II corneal dystrophy
|
C537834 |
|
|
shields type II dentin dysplasia
|
D003784 |
|
|
olivopontocerebellar atrophy II, autosomal recessive
|
9778 |
|
|
pseudohypoaldosteronism, type IIC
|
13778 |
|
|
pseudohypoaldosteronism, type IIC; PHA2C
|
http://purl.obolibrary.org/obo/MONDO_0013778 |
|
|
pseudohypoaldosteronism, type IID
|
13781 |
|
|
pseudohypoaldosteronism, type IID; PHA2D
|
http://purl.obolibrary.org/obo/MONDO_0013781 |
|
|
pseudohypoaldosteronism, type IIE
|
13782 |
|
|
pseudohypoaldosteronism, type IIE; PHA2E
|
http://purl.obolibrary.org/obo/MONDO_0013782 |
|
|
spinocerebellar atrophy III
|
D017827 |
|
