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.
autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency
|
17902 |
|
autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 2 deficiency
|
17902 |
|
nerve injury, mandibular
|
D000080902 |
|
nerve injury, masseteric
|
D000080902 |
|
sarcoma of mast cell
|
19024 |
|
non clonal mast cell activation disorder
|
D000090267 |
|
non clonal mast cell activation syndrome
|
D000090267 |
|
cutaneous (skin) mastocytosis
|
19023 |
|
obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum
|
9023.0 |
|
adenoma of liver cells
|
18902 |
|
susceptibility to nasopharyngeal carcinoma 3
|
http://purl.obolibrary.org/obo/MONDO_0014902 |
|
injury, auriculotemporal nerve
|
D000080902 |
|
injury, buccal nerve
|
D000080902 |
|
injury, mandibular nerve
|
D000080902 |
|
injury, masseteric nerve
|
D000080902 |
|