CUI | Disease | Type | Disease Class | Semantic type | DO Class | HPO Term | Num. genes | Num. SNPs |
---|---|---|---|---|---|---|---|---|
C3661485 | 17p11.2 Monosomy | phenotype | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | Cell or Molecular Dysfunction | 1 | 0 |