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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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meulengracht syndrome
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D005878 |
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syndrome, Gilbert's
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D005878 |
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syndrome, gilbert
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D005878 |
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unconjugated benign bilirubinemia
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D005878 |
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ichthyosis oligophrenia epilepsy syndrome
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C535878 |
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dwarfism ichthyosiform erythroderma mental deficiency syndrome
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C535878 |
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onchocerciasis of eyeball of camera-type eye
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5878 |
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rare disease with autism
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http://purl.obolibrary.org/obo/MONDO_0015878 |
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ichthyosis hypogonadism mental retardation epilepsy syndrome
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C535878 |
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arias type hyperbilirubinemia
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D005878 |
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arias type hyperbilirubinemias
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D005878 |
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ichthyosis male hypogonadism syndrome
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C535878 |
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familial nonhemolytic jaundice
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D005878 |
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ichthyosis mental retardation-epilepsy hypogonadism syndrome
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C535878 |
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neuroichthyosis hypogonadism syndrome
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C535878 |
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