Search results for tcirg1

49 hits were found for tcirg1

# Family MCID Name MIFTS Score
1
c OST126 Osteopetrosis, Autosomal Recessive 1 49 7.125
2
P OST001 Osteopetrosis 70 5.070
3
P NTR004 Neutropenia 63 3.160
4
c ATS282 Autosomal Recessive Malignant Osteopetrosis 37 2.903
5
END081 Endosteal Hyperostosis, Autosomal Dominant 60 2.633
6
c OST134 Osteopetrosis, Autosomal Recessive 6 46 2.594
7
P APL001 Aplastic Anemia 74 2.548
8
P OST002 Osteoporosis 74 2.548
9
P RNL007 Renal Tubular Acidosis 51 2.548
10
LGH007 Leigh Syndrome 70 1.908
11
MTC146 Mitochondrial Complex I Deficiency, Nuclear Type 1 60 1.908
12
c NTR047 Neutropenia, Severe Congenital, 1, Autosomal Dominant 36 1.908
13
c OST136 Osteopetrosis, Autosomal Recessive 7 49 1.862
14
DYS045 Dysosteosclerosis 36 1.862
15
c SVR012 Severe Congenital Neutropenia Autosomal Dominant 28 1.862
16
P CRN052 Craniometaphyseal Dysplasia, Autosomal Dominant 61 1.802
17
PYC001 Pycnodysostosis 56 1.802
18
c OST163 Osteopetrosis, Autosomal Recessive 3 55 1.802
19
CFF003 Caffey Disease 54 1.802
20
c OST131 Osteopetrosis, Autosomal Dominant 2 53 1.802
21
c OST137 Osteopetrosis, Autosomal Recessive 4 45 1.802
22
c OST120 Osteopetrosis, Autosomal Recessive 5 45 1.802
23
c OST129 Osteopetrosis, Autosomal Recessive 2 44 1.802
24
P CRN013 Craniodiaphyseal Dysplasia 41 1.802
25
MNT192 Mental Retardation, X-Linked, Syndromic, Hedera Type 40 1.802
26
c OST106 Osteopetrosis, Autosomal Recessive 8 35 1.802
27
AXL003 Axial Osteomalacia 29 1.802
28
BNR001 Bone Remodeling Disease 28 1.802
29
FBR010 Fibrogenesis Imperfecta Ossium 22 1.802
30
BNR002 Bone Resorption Disease 48 0.228
31
P BND020 Bone Disease 59 0.161
33
c SVR003 Severe Congenital Neutropenia 59 0.125
34
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.102
35
ATS010 Autosomal Recessive Disease 48 0.102
36
RRG015 Rare Genetic Bone Disease 8 0.102
37
PLM001 Pulmonary Tuberculosis 69 0.072
38
P PLM037 Pulmonary Hypertension 67 0.072
39
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.072
40
c BRN108 Branchiootic Syndrome 1 62 0.072
41
P STR020 Strabismus 55 0.072
42
P RTN016 Retinal Degeneration 53 0.072
43
OST011 Osteomalacia 52 0.072
44
PTH003 Pathologic Nystagmus 52 0.072
45
P HYP265 Hypotonia 43 0.072
46
MCH006 Mechanical Strabismus 42 0.072
47
THR035 Thrombasthenia 40 0.072
48
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.072
49
DGN006 Digenic Disease 25 0.072
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