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Oral-facial-digital syndrome 3
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C557817 |
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familial thoracic 3 aortic aneurysm
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C537783 |
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posterior polymorphous, 3 corneal dystrophy
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C563788 |
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fuchs endothelial, 3 corneal dystrophy
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C567678 |
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optic atrophy 3, autosomal recessive
|
9787 |
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deficiency of 3-beta-hydroxysteroid-delta(5)-desaturase
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C537880 |
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spastic paraplegia 39, autosomal recessive
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12787 |
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synpolydactyly, 3, 3-prime, 4, associated with metacarpal and metatarsal synostoses
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C564278 |
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spastic paraplegia 39, autosomal recessive; SPG39
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http://purl.obolibrary.org/obo/MONDO_0012787 |
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fibromatosis, gingival, 3; GINGF3
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http://purl.obolibrary.org/obo/MONDO_0012378 |
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Joubert syndrome 3; JBTS3
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http://purl.obolibrary.org/obo/MONDO_0012078 |
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mirror movements 3; MRMV3
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http://purl.obolibrary.org/obo/MONDO_0014478 |
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