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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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hereditary neuropathy with liability to pressure palsies
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0008087 |
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oculocerebrocutaneous syndrome
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0008108 |
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oculodentodigital dysplasia
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0008111 |
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ophthalmoplegia-intellectual disability-lingua scrotalis syndrome
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0008130 |
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progressive osseous heteroplasia
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0008153 |
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Andersen-Tawil syndrome
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0008222 |
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piebaldism
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0008244 |
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pigmented purpuric eruption
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0008248 |
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autosomal dominant medullary cystic kidney disease with or without hyperuricemia
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0008264 |
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generalized juvenile polyposis/juvenile polyposis coli
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0008276 |
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acute intermittent porphyria
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0008294 |
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ABri amyloidosis
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0008306 |
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contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A
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0008338 |
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Axenfeld-Rieger syndrome type 1
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0008386 |
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spastic paraplegia-epilepsy-intellectual disability syndrome
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0008439 |
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