Search results for HK1

50 hits were found for HK1

# Family MCID Name MIFTS Score
1
HML052 Hemolytic Anemia, Nonspherocytic, Due to Hexokinase Deficiency 26 5.579
2
NRP010 Neuropathy, Hereditary Motor and Sensory, Russe Type 36 5.207
3
NRD073 Neurodevelopmental Disorder with Visual Defects and Brain Anomalies 18 4.457
4
c RTN195 Retinitis Pigmentosa 79 21 4.369
5
P HML002 Hemolytic Anemia 63 4.239
6
P RTN008 Retinitis Pigmentosa 79 3.834
7
P NRP001 Neuropathy 56 3.715
8
P DBT009 Diabetes Mellitus 64 3.218
9
P CHR071 Charcot-Marie-Tooth Disease 65 2.673
10
HYP060 Hyperinsulinism 54 2.673
11
c AMY091 Amyotrophic Lateral Sclerosis 1 89 2.627
12
c HYP595 Hypertension, Essential 84 2.627
13
P ATT013 Attention Deficit-Hyperactivity Disorder 65 2.627
14
ATS010 Autosomal Recessive Disease 48 2.627
15
FND002 Fundus Dystrophy 55 2.167
16
c INH030 Inherited Retinal Disorder 51 2.167
17
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 1.858
18
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 1.858
19
P MTR004 Maturity-Onset Diabetes of the Young 65 1.858
20
c HYP740 Hyperlipoproteinemia, Type V 53 1.858
21
c CNG189 Congenital Disorder of Glycosylation, Type Ib 52 1.858
22
PRD004 Prediabetes Syndrome 47 1.858
23
FRC005 Fructosuria, Essential 39 1.858
24
FTN001 Fat Necrosis of Breast 24 1.858
25
c BCT001 Bacterial Esophagitis 20 1.858
26
P NSP012 Nasopharyngeal Carcinoma 66 0.143
27
RTN023 Retinitis 46 0.143
28
NRR001 Neuroretinitis 42 0.143
29
P GST053 Gastric Cancer 83 0.101
30
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 0.101
31
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 33 0.101
32
NRL016 Neural Tube Defects 82 0.071
33
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.071
34
HYP056 Hypoglycemia 66 0.071
35
PRT037 Pertussis 65 0.071
36
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.071
37
P ANR048 Aniridia 1 63 0.071
38
c WLM018 Wilms Tumor 5 61 0.071
39
SNS003 Sensory Peripheral Neuropathy 54 0.071
40
P RTN016 Retinal Degeneration 53 0.071
41
P RTN018 Retinal Disease 53 0.071
42
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 53 0.071
43
MYL020 Myelomeningocele 51 0.071
44
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 50 0.071
45
c CHR516 Charcot-Marie-Tooth Disease, Type 4c 50 0.071
46
TTH006 Tooth Disease 46 0.071
47
c CHR376 Charcot-Marie-Tooth Disease, Type 4d 46 0.071
48
c ACT202 Acth-Independent Macronodular Adrenal Hyperplasia 2 36 0.071
49
CHR178 Chromosomal Triplication 35 0.071
50
CHR182 Chromosome 10p Duplication 19 0.071
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