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| created at |
2025-11-26 04:53:50 UTC |
| updated at |
2025-11-27 01:00:35 UTC |
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Mondo ID - Mondo Label
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30,114 entries
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There is 0 pattern entry.
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Mobius syndrome
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0008006 |
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MOMO syndrome
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0008008 |
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autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures
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0008026 |
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MYH7-related skeletal myopathy
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0008050 |
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Carney complex, type 1
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0008057 |
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Schilbach-Rott syndrome
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0008113 |
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Feingold syndrome type 1
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0008115 |
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OSLAM syndrome
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0008139 |
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Thiemann disease, familial form
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0008142 |
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Ollier disease
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0008145 |
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Peyronie disease
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0008231 |
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Poland syndrome
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0008262 |
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Cronkhite-Canada syndrome
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0008283 |
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Greig cephalopolysyndactyly syndrome
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0008287 |
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Prader-Willi syndrome
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0008300 |
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