All terms in MONDO
| Label |
Id |
Description |
|
immunoglobulin beta deficiency
|
MONDO_0000583 |
|
|
ataxia-telangiectasia-like disorder 1
|
MONDO_0024557 |
|
|
epilepsy, familial focal, with variable foci 1
|
MONDO_0024556 |
|
|
aortic aneurysm, familial thoracic 1
|
MONDO_0024559 |
|
|
radioulnar synostosis with amegakaryocytic thrombocytopenia 1
|
MONDO_0024558 |
|
|
primary immunodeficiency syndrome due to p14 deficiency
|
MONDO_0012559 |
|
|
obsolete immunoglobulin alpha deficiency
|
MONDO_0000582 |
|
|
obsolete lambda 5 deficiency
|
MONDO_0000581 |
|
|
X-linked lymphoproliferative disease due to SH2D1A deficiency
|
MONDO_0024551 |
|
|
obsolete CD40 ligand deficiency
|
MONDO_0000580 |
|
|
frontometaphyseal dysplasia 1
|
MONDO_0024550 |
|
|
branchiootorenal syndrome 2
|
MONDO_0012575 |
|
|
supranuclear palsy, progressive, 3
|
MONDO_0012576 |
|
|
vesicoureteral reflux 2
|
MONDO_0012573 |
|
|
Potocki-Lupski syndrome
|
MONDO_0012574 |
|
|
autoimmune pulmonary alveolar proteinosis
|
MONDO_0012579 |
|
|
asthma-related traits, susceptibility to, 4
|
MONDO_0012577 |
|
|
autism, susceptibility to, 13
|
MONDO_0012578 |
|
|
choroidal dystrophy, central areolar, 1
|
MONDO_0024539 |
|
|
basal ganglia calcification, idiopathic, 1
|
MONDO_0024538 |
|
