|
OPCA II, Fickler-Winkler type
|
9778 |
|
|
AL-Gazali-BAKALINOVA syndrome; AGBK
|
http://purl.obolibrary.org/obo/MONDO_0011778 |
|
|
nodular lymphocyte-predominant Hodgkin lymphoma
|
44778 |
|
|
CONE-ROD DYSTROPHY AND HEARING LOSS 1
|
20778 |
|
|
leukoderma acquisitum Centrifugum of Sutton
|
6778 |
|
|
lattice type II corneal dystrophy
|
C000657784 |
|
|
olivopontocerebellar atrophy II, autosomal recessive
|
9778 |
|
|
pseudohypoaldosteronism, type IIC
|
13778 |
|
|
pseudohypoaldosteronism, type IIC; PHA2C
|
http://purl.obolibrary.org/obo/MONDO_0013778 |
|
|
intellectual disability Smith Fineman Myers type
|
19778 |
|
|
Smith Fineman Myers syndrome
|
19778 |
|
|
hyperthyroxinemia, dystransthyretinemic; DTTRH
|
http://purl.obolibrary.org/obo/MONDO_0007785 |
|
|
mental retardation Smith Fineman Myers type
|
19778 |
|
|
craniofrontonasal dysplasia, Teebi type
|
7780 |
|
|
cone-rod dystrophy, aipl1-related
|
C565778 |
|
