| manager |
|
| language |
- |
| license |
- |
| created at |
2021-12-22 03:08:20 UTC |
| updated at |
2021-12-22 07:06:09 UTC |
|
MONDO_bioport_pref_name
|
183,974 entries
|
There is 0 pattern entry.
|
autoimmune hypothyroidism
|
C562768 |
|
|
childhood onset IBGC
|
C536276 |
|
|
bilateral striopallidodentate calcinosis, childhood onset
|
C536276 |
|
|
idiopathic, childhood-onset basal ganglia calcification
|
C536276 |
|
|
high-grade neuroendocrine carcinoma of the cervix uteri
|
16276 |
|
|
congenital, 1 capillary malformations
|
C562760 |
|
|
childhood onset bilateral striopallidodentate calcinosis
|
C536276 |
|
|
childhood onset idiopathic basal ganglia calcification
|
C536276 |
|
|
capillary malformations, congenital, 1
|
C562760 |
|
|
high-grade neuroendocrine carcinoma of the uterine cervix
|
16276 |
|
|
idiopathic basal ganglia calcification, childhood onset
|
C536276 |
|
|
nonarteriosclerotic, idiopathic, childhood-onset cerebral calcification
|
C536276 |
|
|
inflammatory myofibroblastic lung tumor
|
6276 |
|
|
genetic defect in, 3 thyroid hormonogenesis
|
C562769 |
|
|
poorly differentiated neuroendocrine carcinoma of the cervix uteri
|
16276 |
|
