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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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combined pituitary hormone deficiencies, genetic form caused by mutation in PROP1
|
9878 |
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arias type hyperbilirubinemia
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D005878 |
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arias type hyperbilirubinemias
|
D005878 |
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congenital generalized hypercontractile muscle stiffness syndrome
|
18780 |
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ichthyosis male hypogonadism syndrome
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C535878 |
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type 1 interferonopathy
|
18782 |
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familial nonhemolytic jaundice
|
D005878 |
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ALS2 amyotrophic lateral sclerosis
|
8780 |
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juvenile amyotrophic lateral sclerosis with dementia
|
8781 |
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penile venous leakage
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D018783 |
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bone dysplasia lethal Holmgren type
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8878 |
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bone dysplasia, lethal Holmgren type
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8878 |
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autosomal recessive lethal chondrodysplasia, round femoral inferior epiphysis type
|
8878 |
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bone dysplasia, lethal, Holmgren type
|
8878 |
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high density lipoprotein deficiency, Tangier type
|
8783 |
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