|
pseudohypoaldosteronism, type IID; PHA2D
|
http://purl.obolibrary.org/obo/MONDO_0013781 |
|
|
systemic Immunoglobulin Light chain amyloidosis
|
17816 |
|
|
ichthyosis hystrix Rheydt type
|
18781 |
|
|
Van Maldergem Wetzburger Verloes syndrome
|
17813 |
|
|
uterine corpus adenomatoid tumor
|
1781 |
|
|
variant ABeta2M amyloidosis
|
17810 |
|
|
primary localized amyloidosis
|
17817 |
|
|
oligodactylous clubfeet, and anonychia-nail hypoplasia syndrome fibular agenesis-hypoplasia
|
C567819 |
|
|
acute bronchitis and bronchiolitis
|
3781 |
|
|
keratitis, ichthyosis, and deafness (KID) syndrome
|
18781 |
|
|
congenital alopecia and nail dystrophy T-cell immunodeficiency
|
C536781 |
|
|
congenital alopecia, and nail dystrophy t-cell immunodeficiency
|
C536781 |
|
