Search results for Foreskin fibroblast (neonatal)

98 hits were found for Foreskin fibroblast (neonatal)

# Family MCID Name MIFTS Score
1
P HRP006 Herpes Simplex 65 0.296
2
PHM001 Phimosis 37 0.270
3
HYP266 Hypoxia 57 0.269
4
P HYP040 Hypospadias 51 0.240
5
48X005 48,xyyy 39 0.227
6
P SYS005 Systemic Scleroderma 68 0.219
7
P TRT010 Teratoma 52 0.212
8
c CHR684 Chronic Kidney Disease 70 0.179
9
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.179
10
SVR004 Severe Combined Immunodeficiency 73 0.177
11
P RTN024 Retinoblastoma 73 0.173
12
c FML008 Familial Retinoblastoma 53 0.173
13
SKN016 Skin Disease 63 0.164
14
CHR178 Chromosomal Triplication 35 0.164
15
CHL123 Chlamydia 59 0.163
16
SRC014 Sarcoma 65 0.161
17
SPN035 Spindle Cell Sarcoma 53 0.159
18
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.152
19
P DBT009 Diabetes Mellitus 64 0.150
20
CHL014 Cholera 59 0.149
21
PPL022 Papilloma 54 0.148
22
IMM167 Immune Deficiency Disease 78 0.143
23
SQM002 Squamous Cell Papilloma 46 0.143
24
HYP457 Hypertrophic Scars 42 0.141
25
P MLN008 Melanoma 69 0.141
26
c ACT068 Acute Cystitis 63 0.139
27
HMN044 Human Immunodeficiency Virus Type 1 71 0.138
28
P LKM002 Leukemia 68 0.137
29
SPN186 Spinal Cord Injury 60 0.136
30
CHC001 Chickenpox 60 0.135
31
SQM006 Squamous Cell Carcinoma 60 0.133
32
P EPD016 Epidermolysis Bullosa 53 0.132
33
CHR100 Chronic Ulcer of Skin 55 0.127
34
HRW001 Hair Whorl 36 0.125
35
OST159 Osteogenic Sarcoma 66 0.125
36
DWR001 Dwarfism 44 0.123
37
P DRM053 Dermatitis, Atopic 66 0.118
38
P GST053 Gastric Cancer 83 0.117
39
LCH016 Lichen Sclerosus Et Atrophicus 41 0.114
40
HYP080 Hypogonadism 50 0.111
41
MSL001 Measles 62 0.108
42
P SYP003 Syphilis 58 0.108
43
P HNT016 Huntington Disease 72 0.107
44
PLY150 Polykaryocytosis Inducer 31 0.104
45
ING001 Inguinal Hernia 60 0.103
46
P GRF003 Graft-Versus-Host Disease 72 0.103
47
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.103
48
ADL002 Adult Syndrome 70 0.101
49
ACQ007 Acquired Immunodeficiency Syndrome 60 0.101
50
GLC003 Glucose Intolerance 54 0.100
51
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.098
52
c BSL007 Basal Cell Carcinoma 68 0.098
53
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.097
54
P RHB003 Rhabdomyosarcoma 63 0.097
55
HMP009 Haemophilus Influenzae 43 0.096
56
PRS045 Prostatic Hypertrophy 53 0.095
57
CRH001 Crohn's Disease 74 0.094
58
CRV035 Cervical Cancer 76 0.094
59
MYL031 Myeloproliferative Neoplasm 66 0.094
60
c DWL002 Dowling-Degos Disease 1 58 0.093
61
NRF007 Neurofibroma 64 0.093
62
KPS004 Kaposi Sarcoma 75 0.092
63
GNT003 Genital Herpes 54 0.092
64
P MYL006 Myeloid Leukemia 60 0.091
65
P AMY004 Amyloidosis 70 0.091
66
CHR619 Chromosome 2q35 Duplication Syndrome 62 0.090
67
c VSC019 Vesicoureteral Reflux 1 57 0.089
68
PLM031 Poliomyelitis 64 0.086
69
BLL006 Bullous Pemphigoid 62 0.083
70
P LMY004 Leiomyosarcoma 63 0.083
71
P LYM118 Lymphoma 68 0.082
72
c PCH010 Pachyonychia Congenita 3 44 0.080
73
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.078
74
VRL011 Viral Infectious Disease 61 0.077
75
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.076
76
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.076
77
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.074
79
c RHB024 Rhabdomyosarcoma 2 67 0.073
80
GST040 Gastric Adenocarcinoma 70 0.073
81
ATX019 Ataxia with Vitamin E Deficiency 42 0.071
82
URT037 Urethral Stricture 43 0.071
83
MLL001 Molluscum Contagiosum 50 0.070
84
CHG001 Chagas Disease 66 0.069
85
P LKM071 Leukemia, Chronic Lymphocytic 79 0.068
86
c LKM063 Leukemia, Chronic Myeloid 72 0.066
87
SKN005 Skin Atrophy 43 0.066
88
LYM133 Lymphoma, Hodgkin, Classic 69 0.062
89
IMP005 Impotence 52 0.059
90
PPL002 Papillary Carcinoma 47 0.057
91
EPD006 Epidermolysis Bullosa Acquisita 49 0.056
92
THR035 Thrombasthenia 40 0.056
93
PYD002 Pyoderma 50 0.052
94
MCR103 Microtia 43 0.052
95
EPD070 Epidermoid Cysts 37 0.052
96
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.051
97
SXL003 Sexual Disorder 47 0.044
98
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.044
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