| 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.
|
corneal crystals myopathy and neuropathy
|
21921 |
|
|
nonsyndromic congenital nail disorder, 4
|
19211 |
|
|
late onset multiple carboxylase deficiency
|
D028921 |
|
|
carboxylase deficiency, multiple, late-onset
|
D028921 |
|
|
hepatopancreatic ampulla neoplasm (disease)
|
921 |
|
|
autosomal recessive nonsyndromic congenital nail disorder-4
|
19211 |
|
|
Estren-Dameshek variant of Fanconi Anemia
|
9215 |
|
|
Estren-Dameshek variant of Fanconi pancytopenia
|
9215 |
|
|
inborn disorder of neurotransmitter metabolism and transport
|
19219 |
|
|
inborn disorder of amino acid absorption and transport
|
19216 |
|
|
inborn error of bile acid biosynthetic process
|
19218 |
|
|
inborn disorder of bile acid synthesis
|
19218 |
|
|
inborn errors of bile acid synthesis
|
19218 |
|
|
inborn error of carbohydrate metabolic process
|
19214 |
|
|
inborn errors of carbohydrate metabolism
|
19214 |
|
