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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.
gorlin syndrome
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D001478 |
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gorlin-goltz syndrome
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D001478 |
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syndrome, gorlin
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D001478 |
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syndrome, gorlin-goltz
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D001478 |
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congenital disorder OF glycosylation, type IIo; CDG2O
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http://purl.obolibrary.org/obo/MONDO_0014789 |
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prolapse, visceral
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D014782 |
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visceral prolapse
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D014782 |
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blindness, day
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D014786 |
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day blindness
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D014786 |
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disabilities, vision
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D014786 |
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disability, vision
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D014786 |
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disorder, visual
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D014786 |
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disorders, visual
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D014786 |
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impairment, visual
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D014786 |
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impairments, visual
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D014786 |
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