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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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familial, 5 alzheimer disease
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C566578 |
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angiopathy, cerebral amyloid
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D016657 |
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sporadic cerebral amyloid angiopathy
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D016657 |
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types 1 and 2 persistent mullerian duct syndrome
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C536665 |
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types i and II persistent mullerian duct syndrome
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C536665 |
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punctate calcifications, and deafness spondylomegaepiphyseal dysplasia with upper limb mesomelia
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C566507 |
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unusual facies, and developmental delay plantar lipomatosis
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C566559 |
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spastic paraplegia and evans syndrome
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C566652 |
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maxillary retrusion, and mental retardation scaphocephaly
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C566511 |
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generalized papular and sclerodermoid
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15665 |
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generalized papular and sclerodermoid lichen myxedematosus
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15665 |
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split hand and split foot with mandibular hypoplasia
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C535665 |
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indeterminate sex and/or pseudohermaphroditism
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24665 |
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cerebral amyloid angiopathies
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D016657 |
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primary open angle glaucoma
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7665 |
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