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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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autosomal recessive limb-girdle muscular dystrophy caused by mutation in ISPD
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14474 |
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autosomal recessive limb-girdle muscular dystrophy due to ISPD deficiency
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14474 |
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autosomal recessive limb-girdle muscular dystrophy type 2U
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14474 |
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muscular dystrophy limb-girdle type 2U
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14474 |
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congenital pigmented melanocytic Nevus
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44792 |
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muscular dystrophy, limb-girdle, type 2U
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14474 |
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erythema multiforme major
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44719 |
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cancer of major salivary gland
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44743 |
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erythema multiforme majus
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44719 |
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carcinoma, endometrial, malignant
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2447 |
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obsolete congenital melanocytic nevus
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44790.0 |
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Giant congenital melanocytic nevus
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44792 |
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large congenital melanocytic nevus
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44792 |
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benign juvenile melanoma
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44793 |
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pituitary stalk meningioma
|
4447 |
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