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| Term | autosomal recessive cutis laxa type II classic type | ID (Ontology) | DOID:0070141 (Human Disease) |
| Definition | A cutis laxa characterized by generalized skin wrinkling, sparse subcutaneous fat, dysmorphic progeroid facial features and severe hypotonia. | ||
| Also Known As | "ARCL2, classic type" ; "ARCL2, Debre type" | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal genetic disease |__autosomal recessive disease__ skin disease | |__cutis laxa___________________| autosomal recessive cutis laxa type II classic type 9 rec. |__autosomal recessive cutis laxa type IIA 5 rec. |__autosomal recessive cutis laxa type IIC 1 rec. |__autosomal recessive cutis laxa type IID 3 rec. |
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| Is a |
autosomal recessive disease cutis laxa |
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External Crossreferences & Linkouts
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ICD10CM:Q82.8 ORDO:357074 |
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