| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
|---|---|---|---|---|
| 10q24.32 | {Medulloblastoma} | 155255 | AD, AR, SMu | 3 |
| {Meningioma, familial, susceptibility to} | 607174 | AD | 3 | |
| Basal cell nevus syndrome 2 | 620343 | 3 | ||
| Joubert syndrome 32 | 617757 | AR | 3 |
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|
|
| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
Gene/Locus |
Gene/Locus MIM number |
|---|---|---|---|---|---|---|
| 9q22.32 | Basal cell nevus syndrome 1 | 109400 | AD | 3 | PTCH1 | 601309 |
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|
|
| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
|---|---|---|---|---|
| 9q22.32 | Basal cell carcinoma, somatic | 605462 | 3 | |
| Basal cell nevus syndrome 1 | 109400 | AD | 3 | |
| Holoprosencephaly 7 | 610828 | AD | 3 |
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