autosomal dominant cutis laxa 3
human disease
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Summary
autosomal dominant cutis laxa 3 is a developmental defect during embryogenesis[1]. It is known by 5 alternative names across languages and contexts.[2]
Key Facts
- autosomal dominant cutis laxa 3's instance of is recorded as developmental defect during embryogenesis[3].
- autosomal dominant cutis laxa 3's instance of is recorded as rare disease[4].
- autosomal dominant cutis laxa 3's instance of is recorded as class of disease[5].
- autosomal dominant cutis laxa 3 is a type of autosomal dominant cutis laxa[6].
- autosomal dominant cutis laxa 3's genetic association is recorded as ALDH18A1[7].
- autosomal dominant cutis laxa 3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0070131[8].
- autosomal dominant cutis laxa 3's exact match is recorded as http://identifiers.org/doid/DOID:0070131[9].
- autosomal dominant cutis laxa 3's on focus list of Wikimedia project is recorded as WikiProject Medicine[10].
Why It Matters
autosomal dominant cutis laxa 3 is known by 5 alternative names across languages and contexts.[2]