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| language |
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| license |
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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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POMT2 autosomal recessive limb-girdle muscular dystrophy
|
13162 |
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autosomal recessive spastic paraplegia type 65
|
13165 |
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dilated cardiomyopathy type 1DD
|
13168 |
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autosomal recessive spastic paraplegia 45
|
13165 |
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5p13 microduplication syndrome
|
13169 |
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gamma aminobutyrate transaminase deficiency
|
13166 |
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gamma-aminobutyric acid transaminase deficiency
|
13166 |
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cardiomyopathy, dilated, type 1Dd
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13168 |
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nephronophthisis-like nephropathy type 1
|
13163 |
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