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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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hereditary sensory and autonomic neuropathy type 1 with cough and gastroesophageal reflux
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11961 |
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hereditary sensory and autonomic neuropathy type 1B
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11961 |
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hereditary sensory and autonomic neuropathy type IB
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11961 |
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HSAN with cough and gastroesophageal reflux
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11961 |
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Joubert syndrome caused by mutation in TMEM216
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11963 |
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heterotopia, periventricular, autosomal recessive
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11966 |
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carbohydrate deficient glycoprotein syndrome type Ih
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11969 |
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periventricular nodular heterotopia 2
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11966 |
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periventricular nodular heterotopia 3
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11967 |
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glucosyltransferase 2 deficiency
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11969 |
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cancer of endometrium
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11962 |
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limb-girdle muscular dystrophy due to alpha-sarcoglycan deficiency
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11968 |
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limb-girdle muscular dystrophy type 2D
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11968 |
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limb-girdle muscular dystrophy, type 2D
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11968 |
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temporal epilepsy, familial
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11965 |
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