Search results for primary hypertrophic osteoarthropathy, autosomal recessive

72 hits were found for primary hypertrophic osteoarthropathy, autosomal recessive

# Family MCID Name MIFTS Score
1
c HYP520 Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 2 23 6.215
2
c HYP793 Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 40 6.143
3
P PRM018 Primary Hypertrophic Osteoarthropathy 46 0.340
4
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.235
5
P ANR048 Aniridia 1 68 0.203
6
ANR038 Anorexia Nervosa 1 21 0.201
7
BLD137 Blood Group--Ahonen 17 0.201
8
P NRP001 Neuropathy 63 0.196
9
P HRT032 Heart Disease 80 0.195
10
TTR025 Tetraamelia Syndrome, Autosomal Recessive 40 0.183
11
HPT082 Hepatic Adenomas, Familial 52 0.183
12
c SCN005 Secondary Hypertrophic Osteoarthropathy 44 0.183
13
END072 Endotheliitis 46 0.181
14
AGN016 Aging 65 0.173
15
P ADN016 Adenocarcinoma 71 0.165
16
SQM006 Squamous Cell Carcinoma 74 0.158
17
ALR002 Al-Raqad Syndrome 30 0.158
18
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.152
19
P ART022 Arthritis 77 0.146
20
P PLM037 Pulmonary Hypertension 79 0.144
21
SRC014 Sarcoma 68 0.135
22
P MYL005 Myelofibrosis 75 0.132
23
P LKM002 Leukemia 75 0.123
24
ALP046 Alport Syndrome, X-Linked 74 0.119
25
PRS047 Prostatitis 59 0.118
26
PRS037 Periostitis 33 0.115
27
P ESP024 Esophagitis 64 0.115
28
P CRV039 Cervicitis 49 0.111
29
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.108
30
P ART023 Arthropathy 68 0.107
31
P LNG032 Lung Cancer 99 0.106
32
P LPS004 Lupus Erythematosus 69 0.096
33
P DBT009 Diabetes Mellitus 72 0.096
34
THR024 Thrombosis 61 0.096
35
P RHM011 Rheumatoid Arthritis 91 0.089
36
P LRY019 Laryngitis 57 0.088
37
P PNM007 Pneumonia 70 0.088
38
P RHB003 Rhabdomyosarcoma 61 0.088
39
P DBT005 Diabetes Insipidus 54 0.087
40
P PRS040 Prostate Cancer 88 0.086
41
NPH003 Nephrocalcinosis 49 0.086
42
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.085
43
LVR012 Liver Cirrhosis 73 0.083
44
P HMN036 Hemangiopericytoma, Malignant 52 0.081
45
P MYC084 Mycobacterium Tuberculosis 1 69 0.079
46
P AGM001 Agammaglobulinemia 70 0.075
47
MYX004 Myxedema 44 0.073
48
OST017 Osteomyelitis 64 0.073
49
P FNC043 Fanconi Anemia, Complementation Group E 52 0.072
50
P ACR062 Acroosteolysis 35 0.072
51
P PTS002 Ptosis 50 0.071
52
c SYS001 Systemic Lupus Erythematosus 86 0.067
53
ACN002 Acanthosis Nigricans 60 0.065
54
PNC001 Pancytopenia 50 0.065
55
PTT046 Pituitary Hormone Deficiency, Combined, 2 57 0.064
56
CRH001 Crohn's Disease 80 0.062
57
c THR092 Thrombophilia Due to Thrombin Defect 61 0.061
58
CLC006 Calcinosis 51 0.060
59
P PTN014 Patent Ductus Arteriosus 1 45 0.056
60
P CTS012 Cutis Verticis Gyrata 22 0.056
61
PTT009 Pituitary Gland Disease 56 0.056
62
PLM017 Pulmonary Alveolar Microlithiasis 48 0.052
63
P SYR001 Syringomyelia 49 0.049
64
CDQ001 Cauda Equina Syndrome 41 0.049
65
BRL012 Bare Lymphocyte Syndrome, Type Ii 57 0.048
66
PLM001 Pulmonary Tuberculosis 72 0.048
67
WBR001 Weber Syndrome 40 0.048
68
MNR003 Mineral Metabolism Disease 33 0.047
69
c CLD010 Cold-Induced Sweating Syndrome 1 47 0.046
70
PLM151 Pulmonary Arteriovenous Fistulas 33 0.043
71
OCL003 Oculomotor Nerve Paralysis 27 0.041
72
THR010 Third Cranial Nerve Disease 26 0.041
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