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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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DNAL4 familial congenital mirror movements
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14478 |
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loss of consciousness
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D014474 |
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pustular dermatitides, contagious
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D004474 |
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pustular dermatitis, contagious
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D004474 |
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nonsyndromic aplasia cutis congenita
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D004476 |
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congenital hepatic cyst
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447 |
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x-linked 5 deafness
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C564472 |
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autosomal dominant deafness 65
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14470 |
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diarrhea from decreased bowel motility
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44763 |
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congenital ectodermal defects
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D004476 |
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type i, deficiency of 11-beta-hydroxysteroid dehydrogenase
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C536447 |
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4q25 proximal deletion syndrome
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44717 |
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contagious pustular dermatitides
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D004474 |
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thyroid gland differentiated carcinoma
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15447 |
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SIN3A-related intellectual disability syndrome due to a point mutation
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44700 |
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