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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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psychomotor retardation, and sensorineural deafness iris dysplasia with ocular hypertelorism
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C566234 |
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aniridia, microcornea, and spontaneously reabsorbed cataract
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C566280 |
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alpha-1-Antitrypsin deficiency, autosomal recessive
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C566273 |
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familial, 4 atrial fibrillation
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C566244 |
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secundum type atrial septal defect
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C566241 |
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ASD with atrioventricular conduction defects
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C566238 |
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sveinsson chorioretinal atrophy
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C566236 |
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erythroreticulosis, hereditary benign
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C566285 |
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metatarsus adductus, and developmental delay brachmann-de lange-like facial changes with microcephaly
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C566206 |
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type i, autosomal recessive bpes
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C566222 |
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long-thumb type brachydactyly
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C566204 |
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early-onset, with cerebral amyloid angiopathy alzheimer disease
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C566299 |
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adult i blood group phenotype
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C566214 |
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adult i blood group with congenital cataract
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C566214 |
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adult i blood group without congenital cataract
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C566214 |
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