Search results for H4C13
13 hits were found for H4C13
# | Family | MCID | Name | MIFTS | Score | |
---|---|---|---|---|---|---|
1 | P | NNN008 | Noonan Syndrome 1 | 76 | 3.062 | |
2 | P | MRG008 | Meier-Gorlin Syndrome 1 | 55 | 3.062 | |
3 | c | LKM061 | Leukemia, Acute Myeloid | 84 | 2.165 | |
4 | P | RTN008 | Retinitis Pigmentosa | 79 | 2.165 | |
5 | CHR593 | Chromosome 16p13.3 Deletion Syndrome, Proximal | 66 | 2.165 | ||
6 | c | HYP604 | Hyperinsulinemic Hypoglycemia, Familial, 2 | 65 | 2.165 | |
7 | c | HYP794 | Hyperoxaluria, Primary, Type I | 63 | 2.165 | |
8 | P | PRM002 | Primary Hyperoxaluria | 62 | 2.165 | |
9 | c | HYP304 | Hyperinsulinemic Hypoglycemia, Familial, 1 | 61 | 2.165 | |
10 | c | HYP601 | Hyperinsulinemic Hypoglycemia, Familial, 3 | 52 | 2.165 | |
11 | NTM002 | Nut Midline Carcinoma | 44 | 2.165 | ||
12 | P | BCL004 | B-Cell Non-Hodgkin Lymphoma | 44 | 2.165 | |
13 | CRB025 | Carbohydrate Metabolic Disorder | 41 | 2.165 |