Search results for HLX

60 hits were found for HLX

# Family MCID Name MIFTS Score
1
c DPH024 Diaphragmatic Hernia, Congenital 64 11.161
2
DPH029 Diaphragmatic Hernia-Short Bowel-Asplenia Syndrome 3 9.408
3
PTN001 Patent Foramen Ovale 62 9.332
4
OVR051 Ovarian Endodermal Sinus Tumor 36 8.918
5
OVR056 Ovarian Primitive Germ Cell Tumor 20 8.918
6
P LYM118 Lymphoma 69 1.736
7
c LKM061 Leukemia, Acute Myeloid 83 1.714
8
LYM133 Lymphoma, Hodgkin, Classic 74 1.692
9
P BRS047 Breast Cancer 97 1.333
10
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 1.284
11
c LKM005 Leukemia, T-Cell, Chronic 33 1.284
13
DFF005 Diffuse Large B-Cell Lymphoma 55 1.227
14
P BCL017 B-Cell Lymphoma 57 1.227
15
P GST053 Gastric Cancer 82 1.197
16
GLC003 Glucose Intolerance 53 1.197
17
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.197
18
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.197
19
PLC005 Placental Insufficiency 56 1.197
20
P ANP001 Anaplastic Large Cell Lymphoma 61 1.163
21
P MYL006 Myeloid Leukemia 60 1.163
22
PLY150 Polykaryocytosis Inducer 29 1.127
23
THY030 Thyroid Gland Disease 50 1.127
24
P HYP086 Hypothyroidism 69 1.127
25
P GRV001 Graves' Disease 54 1.127
26
P RTN024 Retinoblastoma 72 1.087
27
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.042
28
ALL014 Allergic Encephalomyelitis 34 1.042
29
BCT022 Bacterial Infectious Disease 56 0.988
30
SPC026 Specific Granule Deficiency 1 31 0.988
31
NTR011 Neutrophil-Specific Granule Deficiency 36 0.988
32
PLM001 Pulmonary Tuberculosis 69 0.918
33
P OVR042 Ovarian Cancer 88 0.551
34
P PNC035 Pancreatic Cancer 86 0.551
35
CYT002 Cytokine Deficiency 43 0.479
36
MYL009 Myelodysplastic Syndrome 67 0.293
37
FRY002 Fryns Syndrome 39 0.293
38
P HYD006 Hydrocephalus 63 0.293
39
HYD048 Hydrocephalus with Stenosis of the Aqueduct of Sylvius 37 0.293
40
MRG003 Marginal Zone B-Cell Lymphoma 52 0.239
41
SPL004 Splenic Marginal Zone Lymphoma 50 0.239
42
CHR226 Chromosome 1q41-Q42 Deletion Syndrome 30 0.239
43
CHL014 Cholera 62 0.239
44
PRP016 Paraplegia 52 0.239
45
QDR001 Quadriplegia 49 0.239
46
c RTN041 Retinitis Pigmentosa 11 43 0.239
47
c CNG216 Congenital Hydrocephalus 50 0.239
48
SPN186 Spinal Cord Injury 61 0.239
49
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.169
50
P AST005 Asthma 76 0.169
51
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.169
52
P LKM062 Leukemia, Acute Lymphoblastic 69 0.169
53
MNT001 Mantle Cell Lymphoma 65 0.169
54
P FLL037 Follicular Lymphoma 73 0.169
55
BLR001 Biliary Atresia 55 0.169
56
P LKM002 Leukemia 66 0.169
57
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 0.169
58
SPS057 Spasticity 43 0.169
59
PTH003 Pathologic Nystagmus 52 0.169
60
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 0.169
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