Search results for HK1

48 hits were found for HK1

# Family MCID Name MIFTS Score
1
HML052 Hemolytic Anemia, Nonspherocytic, Due to Hexokinase Deficiency 26 5.708
2
NRP010 Neuropathy, Hereditary Motor and Sensory, Russe Type 34 5.328
3
c RTN195 Retinitis Pigmentosa 79 21 4.471
4
P HML002 Hemolytic Anemia 62 4.338
5
P RTN008 Retinitis Pigmentosa 77 3.924
6
P NRP001 Neuropathy 56 3.803
7
NRD073 Neurodevelopmental Disorder with Visual Defects and Brain Anomalies 17 3.585
8
P DBT009 Diabetes Mellitus 64 3.294
9
P CHR071 Charcot-Marie-Tooth Disease 64 2.736
10
HYP060 Hyperinsulinism 54 2.736
11
c AMY091 Amyotrophic Lateral Sclerosis 1 89 2.689
12
c HYP595 Hypertension, Essential 84 2.689
13
P ATT013 Attention Deficit-Hyperactivity Disorder 64 2.689
14
ATS010 Autosomal Recessive Disease 48 2.689
15
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 1.902
16
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 1.902
17
P MTR004 Maturity-Onset Diabetes of the Young 66 1.902
18
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 55 1.902
19
c HYP740 Hyperlipoproteinemia, Type V 54 1.902
20
PRD004 Prediabetes Syndrome 47 1.902
21
END038 Endocrine Pancreas Disease 35 1.902
22
FTN001 Fat Necrosis of Breast 23 1.902
23
c BCT001 Bacterial Esophagitis 22 1.902
24
RTN023 Retinitis 46 0.145
25
NRR001 Neuroretinitis 43 0.145
26
P GST053 Gastric Cancer 83 0.103
27
P NSP012 Nasopharyngeal Carcinoma 67 0.103
28
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 64 0.103
29
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 36 0.103
30
NRL016 Neural Tube Defects 82 0.073
31
DFC004 Deficiency Anemia 75 0.073
32
HYP056 Hypoglycemia 66 0.073
33
PRT037 Pertussis 65 0.073
34
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.073
35
P ANR048 Aniridia 1 63 0.073
36
c WLM018 Wilms Tumor 5 62 0.073
37
P RTN016 Retinal Degeneration 53 0.073
38
SNS003 Sensory Peripheral Neuropathy 53 0.073
39
P RTN018 Retinal Disease 52 0.073
40
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 52 0.073
41
MYL020 Myelomeningocele 51 0.073
42
c CHR516 Charcot-Marie-Tooth Disease, Type 4c 50 0.073
43
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 48 0.073
44
TTH006 Tooth Disease 46 0.073
45
c CHR376 Charcot-Marie-Tooth Disease, Type 4d 43 0.073
46
c ACT202 Acth-Independent Macronodular Adrenal Hyperplasia 2 36 0.073
47
CHR178 Chromosomal Triplication 35 0.073
48
CHR182 Chromosome 10p Duplication 19 0.073
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