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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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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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xp21 contiguous gene deletion syndrome
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D000075262 |
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congenital, with hypogonadotropic hypogonadism adrenal hypoplasia
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D000075262 |
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X-linked adrenal hypoplasia
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D000075262 |
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congenital adrenal hypoplasias
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D000075262 |
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cytomegalic adrenocortical hypoplasias
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D000075262 |
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scleroatrophic and keratotic dermatosis of limbs
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C537526 |
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familial x linked addison disease
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D000075262 |
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defective biosynthesis of proteodermatan sulfate
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7526 |
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Ehlers-Danlos syndrome progeroid type
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7526 |
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Ehlers-Danlos syndrome, progeroid type
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7526 |
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Ehlers-Danlos syndrome, progeroid type (former)
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7526 |
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Ehlers-Danlos syndrome, spondylodysplastic type, 1; EDSSPD1
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http://purl.obolibrary.org/obo/MONDO_0007526 |
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