All terms in MONDO
| Label |
Id |
Description |
|
Horner syndrome
|
MONDO_0001294 |
|
|
agammaglobulinemia 3, autosomal recessive
|
MONDO_0013288 |
|
|
agammaglobulinemia 4, autosomal recessive
|
MONDO_0013289 |
|
|
alpha 1-antitrypsin deficiency
|
MONDO_0013282 |
|
|
immunodeficiency, common variable, 3
|
MONDO_0013283 |
|
|
COG4-congenital disorder of glycosylation
|
MONDO_0013281 |
|
|
immunodeficiency, common variable, 6
|
MONDO_0013286 |
|
|
agammaglobulinemia 2, autosomal recessive
|
MONDO_0013287 |
|
|
immunodeficiency, common variable, 4
|
MONDO_0013284 |
|
|
immunodeficiency, common variable, 5
|
MONDO_0013285 |
|
|
non-psychogenic polydipsia
|
MONDO_0040872 |
|
|
psychogenic polydipsia
|
MONDO_0040871 |
|
|
chromosome 6q11-q14 deletion syndrome
|
MONDO_0013299 |
|
|
isolated microphthalmia 6
|
MONDO_0013293 |
|
|
dermatitis, atopic, 8
|
MONDO_0013294 |
|
|
glycogen storage disease XV
|
MONDO_0013291 |
|
|
chromosome 4q21 deletion syndrome
|
MONDO_0013292 |
|
|
autosomal dominant limb-girdle muscular dystrophy type 1H
|
MONDO_0013297 |
|
|
chromosome 17q21.31 duplication syndrome
|
MONDO_0013298 |
|
|
dermatitis, atopic, 9
|
MONDO_0013295 |
|
