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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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SPG11 amyotrophic lateral sclerosis
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11196 |
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nonfunctional Endocrine neoplasm
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21119 |
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Usher syndrome type 1E
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11195 |
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menopause - premature
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1119 |
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amyotrophic lateral sclerosis 5
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11196 |
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amyotrophic lateral sclerosis 5, juvenile
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11196 |
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amyotrophic lateral sclerosis 5, juvenile; ALS5
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http://purl.obolibrary.org/obo/MONDO_0011196 |
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amyotrophic lateral sclerosis caused by mutation in SPG11
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11196 |
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amyotrophic lateral sclerosis type 5
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11196 |
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autosomal recessive nonsyndromic deafness 18A
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11192 |
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autosomal recessive nonsyndromic deafness caused by mutation in USH1C
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11192 |
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autosomal recessive nonsyndromic deafness type 18A
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11192 |
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Missouri type of spondyloepimetaphyseal dysplasia
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11198 |
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deafness, autosomal recessive 18
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11192 |
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deafness, autosomal recessive 18A
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11192 |
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