NDNC8
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http://purl.obolibrary.org/obo/MONDO_0011852 |
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COL7A1 inherited isolated nail anomaly
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http://purl.obolibrary.org/obo/MONDO_0011852 |
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nail disorder, nonsyndromic congenital, 8
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http://purl.obolibrary.org/obo/MONDO_0011852 |
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nonsyndromic congenital nail disorder type 8
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http://purl.obolibrary.org/obo/MONDO_0011852 |
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toenail dystrophy, isolated
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http://purl.obolibrary.org/obo/MONDO_0011852 |
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Camptosynpolydactyly, complex
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http://purl.obolibrary.org/obo/MONDO_0011853 |
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CCSPD
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http://purl.obolibrary.org/obo/MONDO_0011853 |
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Camptopolydactyly, disorganization type
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http://purl.obolibrary.org/obo/MONDO_0011853 |
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CAMPTOSYNPOLYDACTYLY, COMPLEX; CCSPD
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http://purl.obolibrary.org/obo/MONDO_0011853 |
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Camptosynpolydactyly, complex
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http://purl.obolibrary.org/obo/MONDO_0011853 |
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secretory diarrhea, myopathy, and deafness
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http://purl.obolibrary.org/obo/MONDO_0011854 |
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secretory diarrhea, myopathy, and deafness
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http://purl.obolibrary.org/obo/MONDO_0011854 |
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granular corneal dystrophy type II
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http://purl.obolibrary.org/obo/MONDO_0011855 |
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granular corneal dystrophy, type 2
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http://purl.obolibrary.org/obo/MONDO_0011855 |
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corneal dystrophy Avellino type
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http://purl.obolibrary.org/obo/MONDO_0011855 |
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