All terms in MONDO
| Label |
Id |
Description |
|
retinitis pigmentosa 26
|
MONDO_0012024 |
|
|
progressive myoclonic epilepsy type 9
|
MONDO_0014685 |
|
|
microcephaly 6, primary, autosomal recessive
|
MONDO_0012029 |
|
|
autoimmune disease, susceptibility to, 2
|
MONDO_0012027 |
|
|
autoimmune disease, susceptibility to, 3
|
MONDO_0012028 |
|
|
Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome
|
MONDO_0014689 |
|
|
herpes simplex encephalitis, susceptibility to, 7
|
MONDO_0014680 |
|
|
combined oxidative phosphorylation defect type 26
|
MONDO_0014684 |
|
|
myopia 17, autosomal dominant
|
MONDO_0012021 |
|
|
orofacial cleft 4
|
MONDO_0012022 |
|
|
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A9
|
MONDO_0014683 |
|
|
thyroid cancer, nonmedullary, 5
|
MONDO_0014682 |
|
|
chromosome 22q11.2 microduplication syndrome
|
MONDO_0012020 |
|
|
partial duplication of the long arm of chromosome 22
|
MONDO_0016972 |
|
|
thyroid cancer, nonmedullary, 4
|
MONDO_0014681 |
|
|
obsolete immunodeficiency with hyper-IgM
|
MONDO_0000047 |
|
|
obsolete hypouricemia, renal
|
MONDO_0000046 |
|
|
obsolete invasive pneumococcal disease, recurrent isolated
|
MONDO_0000049 |
|
|
obsolete immunoglobulin A deficiency
|
MONDO_0000048 |
|
|
obsolete hypomagnesemia
|
MONDO_0000043 |
|
