|
Hirschsprung disease type 3
|
13383 |
|
|
syndrome associated with craniosynostosis
|
15338 |
|
|
reticuloendotheliosis familial with eosinophilia
|
11338 |
|
|
reticuloendotheliosis, familial, with eosinophilia
|
11338 |
|
|
combined immunodeficiency with hypereosinophilia
|
11338 |
|
|
immunodeficiency, common variable, 11
|
14338 |
|
|
immunodeficiency, common variable, 11; CVID11
|
http://purl.obolibrary.org/obo/MONDO_0014338 |
|
|
immunodeficiency, common variable, type 11
|
14338 |
|
|
ampulla of vater clear cell adenocarcinoma
|
3388 |
|
|
episodic recurrent vertigo
|
D020338 |
|
|
episodic recurrent vertigos
|
D020338 |
|
|
nerve inflammation, vestibular
|
D020338 |
|
|
nerve inflammations, vestibular
|
D020338 |
|
|
nerve neuritides, vestibular
|
D020338 |
|
|
nerve neuritis, vestibular
|
D020338 |
|
