| 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.
|
myositis, inclusion body
|
D018979 |
|
|
sporadic inclusion body myopathy
|
D018979 |
|
|
myopathy, inclusion body, sporadic
|
D018979 |
|
|
myositis, inclusion body, sporadic
|
D018979 |
|
|
dystrophic epidermolysis bullosa, dominant neonatal
|
C536979 |
|
|
familial, 2 candidiasis
|
C537979 |
|
|
autosomal recessive candidiasis familial chronic mucocutaneous
|
C537979 |
|
|
papillary epidermoid carcinoma
|
2979 |
|
|
papillary squamous carcinoma
|
2979 |
|
|
ossified EAR cartilages with mental deficiency, muscle wasting, and BONY changes
|
9798 |
|
|
endemic treponematosis caused by Treponema carateum
|
979 |
|
|
papillary epidermoid cell carcinoma
|
2979 |
|
|
papillary squamous cell carcinoma
|
2979 |
|
|
disease by cell type
|
44979.0 |
|
|
autosomal dominant cerebellar ataxia type 1
|
19792 |
|
