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| created at |
2021-12-22 03:08:20 UTC |
| updated at |
2021-12-22 07:06:09 UTC |
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MONDO_bioport_pref_name
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183,974 entries
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There is 0 pattern entry.
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vulvodynia, generalized
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D056650 |
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vulvodynias, generalized
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D056650 |
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rheumatoid vasculitides
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D056653 |
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vasculitides, rheumatoid
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D056653 |
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autosomal dominant 15 deafness
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C566545 |
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autosomal recessive 18 deafness
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C566580 |
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familial restrictive, 2 cardiomyopathy
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C566512 |
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familial febrile, 2 convulsions
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C566541 |
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familial febrile, 2 seizures
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C566541 |
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medium chain 3-Ketoacyl-CoA thiolase deficiency
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C566566 |
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hemochromatosis, type 2b
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C566557 |
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limb-girdle, type 1e muscular dystrophy
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C566589 |
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limb-girdle, type 2g muscular dystrophy
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C566599 |
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familial hemiplegic, 3 migraine
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C566500 |
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parkinson disease 3, autosomal dominant lewy body
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C566552 |
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