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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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alzheimer disease 5
|
C566578 |
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Ring chromosome 5 syndrome
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16654 |
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autosomal dominant Charcot-Marie-Tooth disease type 2 due to NAGLU mutation
|
14665 |
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nodular sclerosis Classic Hodgkin lymphoma
|
4665 |
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autosomal dominant Charcot-Marie-Tooth disease type 2V
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14665 |
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INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 68
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32665 |
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Mental Retardation, Autosomal Recessive 68
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32665 |
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shohat type SEMD
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C566523 |
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nerve paralysis, Facial
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5665 |
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paralysis Of Facial nerve
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5665 |
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missouri type SEMD
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C566574 |
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intellectual disability, X-linked, syndromic 6
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10665 |
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nodular sclerosis Hodgkin lymphoma
|
4665 |
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nodular sclerosis Hodgkin's disease
|
4665 |
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nodular sclerosis Hodgkin's lymphoma
|
4665 |
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