| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
|---|---|---|---|---|
| 10q26.13 | {Macular degeneration, age-related, 7} | 610149 | 3 | |
| {Macular degeneration, age-related, neovascular type} | 610149 | 3 | ||
| CARASIL syndrome | 600142 | AR | 3 | |
| Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2 | 616779 | AD | 3 |
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| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
Gene/Locus |
Gene/Locus MIM number |
|---|---|---|---|---|---|---|
| 10q26.13 | Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2 | 616779 | AD | 3 | HTRA1 | 602194 |
| Location | Phenotype | Inheritance |
Phenotype mapping key |
Phenotype MIM number |
Gene/Locus |
Gene/Locus MIM number |
|---|---|---|---|---|---|---|
| 10q26.13 | Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2 | AD | 3 | 616779 | HTRA1 | 602194 |
| 10q26.13 | CARASIL syndrome | AR | 3 | 600142 | HTRA1 | 602194 |
| 19p13.12 | Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 1 | AD | 3 | 125310 | NOTCH3 | 600276 |
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|
| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
Gene/Locus |
Gene/Locus MIM number |
|---|---|---|---|---|---|---|
| 10q26.13 | CARASIL syndrome | 600142 | AR | 3 | HTRA1 | 602194 |
| Location | Phenotype | Inheritance |
Phenotype mapping key |
Phenotype MIM number |
Gene/Locus |
Gene/Locus MIM number |
|---|---|---|---|---|---|---|
| 10q26.13 | Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2 | AD | 3 | 616779 | HTRA1 | 602194 |
| 10q26.13 | CARASIL syndrome | AR | 3 | 600142 | HTRA1 | 602194 |
| 19p13.12 | Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 1 | AD | 3 | 125310 | NOTCH3 | 600276 |
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