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MIM:212720 - MARTSOLF SYNDROME 1; MARTS1
Xenbase Genes: rab3gap2
Human Disease Resource: MIM
| MONDO:0008929 - obsolete cataract-intellectual disability-hypogonadism syndrome |
| MONDO:8000008 - Martsolf syndrome 1 |
| DOID:0111586 - Martsolf syndrome |
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| MONDO:0008929 - obsolete cataract-intellectual disability-hypogonadism syndrome |
| MONDO:8000008 - Martsolf syndrome 1 |
| DOID:0111586 - Martsolf syndrome |