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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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B4GALT7-CDG
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7526 |
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sclerotylosis
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C537526 |
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bilateral PPD2
|
17526 |
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XGPT deficiency
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7526 |
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huriez syndrome
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C537526 |
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familial hypoadrenocorticism
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D000075262 |
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familial hypoadrenocorticisms
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D000075262 |
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hypoadrenocorticisms, familial
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D000075262 |
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congenital, with hypogonadotropic hypogonadism adrenal hypoplasia
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D000075262 |
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hypoplasia, congenital adrenal
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D000075262 |
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x linked adrenal hypoplasia
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D000075262 |
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galactosyltransferase I deficiency
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7526 |
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xylosylprotein 4-beta-galactosyltransferase deficiency
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7526 |
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x-linked addison disease
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D000075262 |
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familial X-linked addison disease
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D000075262 |
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