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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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obsolete glycoprotein, renal
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7678.0 |
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X-linked mental retardation snyder - robinson type
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C536678 |
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snyder-robinson mental retardation syndrome
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C536678 |
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charlevoix-saguenay type spastic ataxia
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C536787 |
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autosomal recessive spastic ataxia 6
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C536787 |
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autosomal recessive spastic ataxia of charlevoix-saguenay
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C536787 |
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autosomal recessive spastic paraplegia-50
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C567858 |
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senses disorder, special
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D012678 |
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senses disorders, special
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D012678 |
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disorder, autistic spectrum
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D000067877 |
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polyclonal hyperviscosity syndrome
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18678 |
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Fanconi Schlesinger syndrome
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8678 |
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snyder robinson syndrome
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C536678 |
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pignata guarino syndrome
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C536781 |
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CACH VWM syndrome
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D056784 |
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