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
Content
Loading form....