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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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trisomy xpter xq13 x chromosome
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C536731 |
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sensorineural deafness with pituitary dwarfism
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C536710 |
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cone dystrophy with night blindness and supernormal rod responses, KCNV2-Related
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C563678 |
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epilepsy, familial, with nocturnal wandering and ictal fear
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C563679 |
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trisomy xq x chromosome
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C536732 |
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endosteal hyperostosis worth type
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C536748 |
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autosomal dominant worth type with torus palatinus osteosclerosis
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C536748 |
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trisomy xq25 x chromosome
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C536733 |
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monosomy xq28 x chromosome
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C536755 |
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trisomy xp3 x chromosome
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C536756 |
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immunoneurologic disorder, x-linked
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C536743 |
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anemia, sideroblastic, x-linked
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C536761 |
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