Search results for HLX

32 hits were found for HLX

# Family MCID Name MIFTS Score
1
c DPH024 Diaphragmatic Hernia, Congenital 66 3.385
2
c USH037 Usher Syndrome, Type Iia 49 3.292
3
c HLP026 Holoprosencephaly 3 44 3.292
4
OVR112 Ovarian Germ Cell Cancer 43 3.292
5
DPH021 Diaphragm Disease 43 3.292
6
OVR051 Ovarian Endodermal Sinus Tumor 30 3.292
7
OVR056 Ovarian Primitive Germ Cell Tumor 15 3.292
8
DPH029 Diaphragmatic Hernia-Short Bowel-Asplenia Syndrome 3 2.393
9
c LKM061 Leukemia, Acute Myeloid 84 0.112
10
LYM133 Lymphoma, Hodgkin, Classic 70 0.112
11
P MYL006 Myeloid Leukemia 61 0.112
12
P RTN024 Retinoblastoma 74 0.079
13
PLM001 Pulmonary Tuberculosis 72 0.079
14
P HYP086 Hypothyroidism 70 0.079
15
P LYM118 Lymphoma 70 0.079
16
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.079
17
P BCL017 B-Cell Lymphoma 61 0.079
18
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.079
19
BCT022 Bacterial Infectious Disease 57 0.079
20
P GRV001 Graves' Disease 57 0.079
21
DFF005 Diffuse Large B-Cell Lymphoma 56 0.079
22
GLC003 Glucose Intolerance 55 0.079
23
PLC005 Placental Insufficiency 55 0.079
24
THY030 Thyroid Gland Disease 53 0.079
25
P TCL004 T-Cell Leukemia 48 0.079
26
c FML008 Familial Retinoblastoma 46 0.079
27
FRY002 Fryns Syndrome 41 0.079
28
ALL014 Allergic Encephalomyelitis 40 0.079
29
c LKM005 Leukemia, T-Cell, Chronic 35 0.079
30
SPC026 Specific Granule Deficiency 1 30 0.079
31
NTR011 Neutrophil-Specific Granule Deficiency 28 0.079
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