An instance of cutis laxa that is inherited.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Autosomal recessive cutis laxa type 2 | MONDO:0019573 | 5 | |
| Autosomal dominant cutis laxa | MONDO:0019571 | 3 | |
| Autosomal recessive cutis laxa type 1 | MONDO:0019572 | 3 | |
| ALDH18A1-related de Barsy syndrome | MONDO:0009053 | ||
| PYCR1-related de Barsy syndrome | MONDO:0013755 | PYCR1 | |
| RIN2 syndrome | MONDO:0013115 | RIN2 | |
| Arterial tortuosity syndrome | MONDO:0008818 | SLC2A10 | |
| Arterial tortuosity-bone fragility syndrome | MONDO:0971179 | EMILIN1 | |
| Autosomal recessive cutis laxa type 2, classic type | MONDO:0009054 | ||
| Craniofaciofrontodigital syndrome | MONDO:0007259 | ||
| Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies | MONDO:0013170 | LTBP4 | |
| Cutis laxa, autosomal recessive, type 2E | MONDO:0030337 | LTBP1 | |
| Geroderma osteodysplasticum | MONDO:0009271 | GORAB | |
| Occipital horn syndrome | MONDO:0010572 | ATP7A |
Rare disease
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