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created at |
2024-09-19 07:43:07 UTC |
updated at |
2024-09-23 18:19:38 UTC |
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MedGen CUI
Namespace: https://www.ncbi.nlm.nih.gov/medgen/
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622,528 entries
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There is 0 pattern entry.
CUTIS LAXA WITH BONE DYSTROPHY
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C0268355 |
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CUTIS LAXA WITH CONGENITAL DISORDER OF GLYCOSYLATION
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C0268355 |
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cutis laxa, autosomal recessive type 2A
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C0268355 |
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cutis laxa, autosomal recessive, type 2A
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C0268355 |
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cutis laxa, autosomal recessive, type IIA
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C0268355 |
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cutis laxa, debre type
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C0268355 |
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Autosomal recessive cutis laxa type 2A
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C0268355 |
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autosomal recessive cutis laxa type 2A
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C0268355 |
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autosomal recessive cutis laxa type IIA
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C0268355 |
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cutis laxa with bone dystrophy
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C0268355 |
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cutis laxa with Joint laxity and retarded development
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C0268355 |
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cutis laxa with congenital disorder of glycosylation
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C0268355 |
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cutis laxa with growth and developmental delay
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C0268355 |
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Cutis laxa with joint laxity and retarded development
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C0268355 |
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Cutis laxa with osteodystrophy
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C0268355 |
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