Search results for bmp5

112 hits were found for bmp5

# Family MCID Name MIFTS Score
1
OST012 Osteoarthritis 77 19.182
2
KSH001 Keshan Disease 31 11.658
3
NPH010 Nephrosclerosis 50 11.501
4
P OTS001 Otosclerosis 49 8.289
5
c BRC079 Brachydactyly, Type A2 51 8.132
6
c BRC109 Brachydactyly, Type E1 45 8.132
7
c CRD057 Cardiomyopathy, Familial Restrictive, 2 19 8.132
8
c DVL118 Developmental and Epileptic Encephalopathy 94 45 8.132
9
c DYS059 Dystonia 16 48 8.132
10
RNL008 Renal Artery Atheroma 24 8.132
11
P CLR023 Colorectal Cancer 100 1.864
12
P SKN015 Skin Carcinoma 71 1.278
13
OSS012 Osseous Heteroplasia, Progressive 61 1.148
14
FBR011 Fibrodysplasia Ossificans Progressiva 67 1.148
15
P HRS035 Hirschsprung Disease 1 66 1.148
16
BRR014 Barrett Esophagus 66 1.148
17
P MJR001 Major Depressive Disorder 68 0.991
18
MNT002 Mental Depression 56 0.991
19
DPR016 Depression 64 0.991
20
P PNC035 Pancreatic Cancer 87 0.953
21
P BRS047 Breast Cancer 97 0.851
22
P CHR345 Chronic Pain 50 0.834
23
IRN008 Iron Overload in Africa 50 0.418
24
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 57 0.418
25
c HPT073 Hepatitis C Virus 70 0.418
26
RJS001 Ruijs-Aalfs Syndrome 47 0.418
27
P HPT023 Hepatocellular Carcinoma 95 0.418
28
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 0.418
29
ADL096 Adult Hepatocellular Carcinoma 60 0.418
30
HPT079 Hepatoid Adenocarcinoma 39 0.418
31
PDT042 Pediatric Hepatocellular Carcinoma 51 0.418
32
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.418
33
FBR086 Fibrolamellar Carcinoma 59 0.418
34
HPT011 Hepatocellular Clear Cell Carcinoma 46 0.418
35
PTY007 Pityriasis Rotunda 27 0.418
36
P LNG064 Lung Cancer Susceptibility 3 69 0.351
37
P ADN016 Adenocarcinoma 63 0.351
38
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.314
39
PRS129 Prostatic Hyperplasia, Benign 48 0.314
40
SQM006 Squamous Cell Carcinoma 59 0.314
41
PRS021 Prostatic Adenoma 43 0.314
42
LNG039 Lung Squamous Cell Carcinoma 57 0.314
43
PRS045 Prostatic Hypertrophy 53 0.314
44
P THL005 Thalassemia 56 0.314
45
MCR103 Microtia 40 0.314
46
ALV005 Alveolar Soft Part Sarcoma 61 0.222
47
OST159 Osteogenic Sarcoma 66 0.222
48
SRC027 Sarcoma, Synovial 58 0.222
49
c MYS019 Miyoshi Muscular Dystrophy 2 20 0.222
50
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.222
51
ADR016 Adrenal Cortical Carcinoma 61 0.222
52
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.222
53
RCT020 Rectum Adenocarcinoma 48 0.222
54
ADR004 Adrenal Cortical Adenocarcinoma 38 0.222
55
P RHB003 Rhabdomyosarcoma 66 0.222
56
ANH002 Anhidrosis 45 0.222
57
P KLL001 Kallmann Syndrome 65 0.222
58
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.157
59
PRT251 Proteinuria, Chronic Benign 58 0.157
60
ALL003 Allergic Rhinitis 66 0.157
61
TRC062 Tricuspid Atresia 54 0.157
62
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.157
63
c VSC019 Vesicoureteral Reflux 1 56 0.157
64
CNT061 Conotruncal Heart Malformations 66 0.157
65
PPL052 Papillomatosis, Confluent and Reticulated 34 0.157
66
OTT002 Otitis Media 70 0.157
67
P OVR042 Ovarian Cancer 88 0.157
68
c SML038 Small Cell Cancer of the Lung 68 0.157
69
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 0.157
70
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.157
71
ATS010 Autosomal Recessive Disease 42 0.157
72
P GST053 Gastric Cancer 82 0.157
73
P MRG008 Meier-Gorlin Syndrome 1 55 0.157
74
c HMC039 Hemochromatosis, Type 1 73 0.157
75
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.157
76
c HYP521 Hypogonadotropic Hypogonadism 10 with or Without Anosmia 26 0.157
77
SMT018 Smith-Mccort Dysplasia 2 34 0.157
78
P MGL010 Megalencephalic Leukoencephalopathy with Subcortical Cysts 2a 39 0.157
79
c ATR087 Atrial Standstill 1 74 0.157
80
c BRC081 Brachydactyly, Type C 50 0.157
81
CLF027 Cleft Palate, Isolated 64 0.157
82
BNR002 Bone Resorption Disease 47 0.157
83
ANT039 Antisynthetase Syndrome 55 0.157
84
P PRS049 Persistent Mullerian Duct Syndrome 51 0.157
85
P VNT002 Ventricular Septal Defect 58 0.157
86
GLB002 Glioblastoma 67 0.157
87
HMS001 Hemosiderosis 48 0.157
88
P MLN007 Male Infertility 56 0.157
89
HRT011 Heart Septal Defect 49 0.157
90
P PLY011 Polycystic Ovary Syndrome 57 0.157
91
P URN019 Urinary Tract Infection 48 0.157
92
P EPL164 Epilepsy 70 0.157
93
ENC005 Encephalomalacia 43 0.157
94
P RHN004 Rhinitis 56 0.157
95
P HLP001 Holoprosencephaly 68 0.157
96
GST033 Gestational Diabetes 60 0.157
97
c PRC016 Pre-Eclampsia 64 0.157
98
PRM013 Premature Menopause 57 0.157
99
PLC008 Placenta Disease 48 0.157
100
CLF001 Cleft Lip 54 0.157
101
GLM045 Glioma 62 0.157
102
P HYP055 Hypoplastic Left Heart Syndrome 65 0.157
103
ALL014 Allergic Encephalomyelitis 34 0.157
104
48X005 48,xyyy 39 0.157
105
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.157
106
c LKM005 Leukemia, T-Cell, Chronic 33 0.157
107
CLF056 Cleft Lip with or Without Cleft Palate 43 0.157
108
ANX004 Anoxia 40 0.157
109
P RRH023 Rare Hereditary Hemochromatosis 52 0.157
110
SNG003 Single Ventricular Heart 30 0.157
111
SPN186 Spinal Cord Injury 60 0.157
112
GLL048 Glial Tumor 51 0.157
Content
Loading form....