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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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Anisospondylic camptomicromelic dwarfism Silverman-Handmaker type
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9140 |
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lethal congenital dwarfism with accelerated skeletal maturation
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C537914 |
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Anisospondylic Camptomicromelic dwarfism, Silverman-Handmaker type
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9140 |
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oculopharyngeal muscular dystrophies
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D039141 |
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fiber type disproportion myopathy, congenital
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D020914 |
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congenital fiber-type disproportions
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D020914 |
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hereditary thrombophilia due to PC deficiency
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19145 |
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progressive muscular dystrophy, oculopharyngeal type
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D039141 |
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hereditary thrombophilia due to congenital protein C deficiency
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19145 |
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hereditary thrombophilia due to congenital protein S deficiency
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19144 |
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extraoral halitosis due to methanethiol oxidase deficiency
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29144 |
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cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
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914 |
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keratosis palmoplantaris-cystic eyelids-hypodontia-hypotrichosis syndrome
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9145 |
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centronuclear, autosomal dominant myopathy
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D020914 |
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hemorrhagic fever, ebola
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D019142 |
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