| manager |
|
| language |
- |
| license |
- |
| created at |
2021-12-20 02:12:37 UTC |
| updated at |
2021-12-22 07:05:13 UTC |
|
MONDO_prefferred_names from the Bioportal site.
|
24,286 entries
|
There is 0 pattern entry.
|
early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome
|
44646.0 |
|
|
Bardet-Biedl syndrome 18
|
14446.0 |
|
|
angioleiomyoma
|
6646.0 |
|
|
orthostatic hypotensive disorder, Streeten type
|
7746.0 |
|
|
olfactory groove meningioma
|
4446.0 |
|
|
mental retardation, autosomal recessive 64
|
20846.0 |
|
|
ectodermal dysplasia-sensorineural deafness syndrome
|
9146.0 |
|
|
zoonotic bacterial infection
|
44746.0 |
|
|
KBG syndrome
|
7846.0 |
|
|
gamma-heavy chain disease
|
15046.0 |
|
|
ventricular septal defect 1
|
13746.0 |
|
|
autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome
|
18446.0 |
|
|
ferro-cerebro-cutaneous syndrome
|
18346.0 |
|
|
localized lichen myxedematosus
|
19446.0 |
|
|
peripartum cardiomyopathy, susceptibility to
|
13846.0 |
|
