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| created at |
2024-09-19 07:43:07 UTC |
| updated at |
2024-09-23 18:19:38 UTC |
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MedGen CUI
Namespace: https://www.ncbi.nlm.nih.gov/medgen/
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622,528 entries
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There is 0 pattern entry.
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X-linked intellectual disability-hypotonia syndrome
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C0795889 |
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MCT8-specific thyroid hormone cell Membrane transporter deficiency
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C0795889 |
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intellectual disability, X-linked, with hypotonia
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C0795889 |
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mental retardation, X-linked, with hypotonia
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C0795889 |
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Monocarboxylate transporter-8 deficiency
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C0795889 |
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monocarboxylate transporter-8 deficiency
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C0795889 |
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Mental retardation and muscular atrophy
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C0795889 |
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intellectual disability and muscular atrophy
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C0795889 |
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mental retardation and muscular atrophy
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C0795889 |
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X-linked mental retardation with hypotonia
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C0795889 |
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