Search results for "primary hypertrophic osteoarthropathy, autosomal recessive"

The MalaCard for "primary hypertrophic osteoarthropathy, autosomal recessive" has been retired.
Searching MalaCards for entries containing "primary hypertrophic osteoarthropathy, autosomal recessive"

112 hits were found for 'primary hypertrophic osteoarthropathy, autosomal recessive'

# Family MCID Name MIFTS Score
1
CRN246 Cranioosteoarthropathy 31 6.374
2
c HYP533 Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 25 6.030
3
P PRM018 Primary Hypertrophic Osteoarthropathy 42 0.317
4
P HRT032 Heart Disease 75 0.187
5
P NRP001 Neuropathy 59 0.184
6
HPT074 Hepatic Adenoma, Somatic 50 0.168
7
END072 Endotheliitis 42 0.167
8
HNM002 Hinman Syndrome 25 0.166
9
TTR016 Tetra-Amelia Syndrome 36 0.158
10
P ADN016 Adenocarcinoma 69 0.146
11
SQM006 Squamous Cell Carcinoma 70 0.142
12
P ART022 Arthritis 75 0.136
13
P MSC007 Muscle Hypertrophy 58 0.126
14
AND005 Androgen Insensitivity Syndrome, Mild 16 0.123
15
P MYL005 Myelofibrosis 67 0.122
16
P ESP024 Esophagitis 61 0.110
17
PRS047 Prostatitis 56 0.109
18
P LKM002 Leukemia 71 0.108
19
TTH006 Tooth Disease 52 0.106
20
PRS037 Periostitis 30 0.105
21
P ART023 Arthropathy 64 0.101
22
P LNG032 Lung Cancer 95 0.094
23
P RHM011 Rheumatoid Arthritis 89 0.092
24
P CRV039 Cervicitis 45 0.090
25
JNT002 Joint Disorders 55 0.090
26
P LPS004 Lupus Erythematosus 64 0.088
27
VSC011 Vasculitis 62 0.086
28
THR024 Thrombosis 57 0.085
29
TBR010 Tuberculosis 70 0.084
30
P LRY019 Laryngitis 54 0.084
31
P PNM007 Pneumonia 68 0.083
32
P CHR071 Charcot-Marie-Tooth Disease 67 0.083
33
NPH003 Nephrocalcinosis 48 0.082
34
HYP006 Hypertensive Heart Disease 50 0.081
35
BRT030 Birth Defects 43 0.078
36
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.077
37
OST017 Osteomyelitis 61 0.076
38
ACR007 Acromegaly 66 0.075
39
ACR041 Acromelic Frontonasal Dysostosis 45 0.074
40
LVR012 Liver Cirrhosis 67 0.074
41
LYM019 Lymphosarcoma 53 0.074
42
DJR004 Dejerine-Sottas Disease 46 0.071
43
P FNC043 Fanconi Anemia, Complementation Group E 55 0.070
44
P PTS002 Ptosis 51 0.068
45
SPN051 Spondylitis 51 0.067
46
P AGM001 Agammaglobulinemia 64 0.066
47
ACN002 Acanthosis Nigricans 57 0.065
48
PRP019 Peripheral Nervous System Disease 55 0.065
49
P FBR017 Fibrosarcoma 56 0.065
50
P PTN002 Patent Ductus Arteriosus 52 0.064
51
PLN005 Palindromic Rheumatism 43 0.064
52
OTT002 Otitis Media 66 0.063
53
c SYS001 Systemic Lupus Erythematosus 86 0.061
54
P PNC001 Pancytopenia 52 0.061
55
c THR092 Thrombophilia Due to Thrombin Defect 54 0.060
56
CRH001 Crohn's Disease 75 0.060
57
P CHR102 Charcot-Marie-Tooth Neuropathy 41 0.060
58
CDQ001 Cauda Equina Syndrome 41 0.059
59
ADR038 Adermatoglyphia 46 0.059
60
c CHR350 Charcot-Marie-Tooth Disease, Axonal, Type 2k 36 0.059
61
P ANR007 Anorexia Nervosa 61 0.057
62
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 35 0.057
63
P GT001 Gout 58 0.057
64
c CHR536 Charcot-Marie-Tooth Disease, Type 1a 58 0.057
65
ESP021 Esophageal Cancer 76 0.057
66
RSS002 Roussy-Levy Syndrome 50 0.056
67
RGH009 Right Atrial Isomerism 44 0.056
68
NRP016 Neuropathy, Recurrent, with Pressure Palsies 38 0.056
69
c HRD088 Hereditary Neuropathies 40 0.056
70
c NRP037 Neuropathy, Hereditary Sensory and Autonomic, Type V 54 0.056
71
DBT010 Diabetic Neuropathy 55 0.054
72
c CHR527 Charcot-Marie-Tooth Disease, Type 1b 49 0.054
73
c CLD010 Cold-Induced Sweating Syndrome 1 42 0.053
74
P HMN036 Hemangiopericytoma, Malignant 42 0.053
75
c CHR532 Charcot-Marie-Tooth Disease, Type 2e 49 0.053
76
PMS001 Poems Syndrome 52 0.053
77
NRP015 Neuropathy, Congenital Hypomyelinating 52 0.053
78
P CHR348 Charcot-Marie-Tooth Neuropathy, X-Linked Dominant, 1 38 0.052
79
PLM001 Pulmonary Tuberculosis 67 0.051
80
c CHR407 Charcot-Marie-Tooth Disease, Type 4f 38 0.051
81
c CHR520 Charcot-Marie-Tooth Disease, Axonal, Type 2s 36 0.051
82
KSH004 Kashin-Beck Disease 33 0.051
83
P PLZ001 Pelizaeus-Merzbacher Disease 65 0.051
84
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 43 0.050
85
P HRD021 Hereditary Sensory Neuropathy 46 0.049
86
SNS003 Sensory Peripheral Neuropathy 45 0.049
87
ATN004 Autonomic Neuropathy 45 0.048
88
P THL005 Thalassemia 64 0.048
89
AMB002 Amblyopia 46 0.048
90
c CHR374 Charcot-Marie-Tooth Neuropathy, X-Linked Recessive, 3 31 0.048
91
c CHR530 Charcot-Marie-Tooth Disease, Type 2b 40 0.047
92
c HRD094 Hereditary Motor and Sensory Neuropathy, Type Iic 34 0.047
93
c CHR535 Charcot-Marie-Tooth Disease, Type 1c 37 0.047
94
c CHR533 Charcot-Marie-Tooth Disease, Type 1f 36 0.046
95
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 33 0.046
96
PLM017 Pulmonary Alveolar Microlithiasis 46 0.046
97
ART005 Arteriovenous Malformation 66 0.046
98
c CHR537 Charcot-Marie-Tooth Disease, Type 1e 50 0.046
99
MTR007 Motor Peripheral Neuropathy 37 0.046
100
c CHR352 Charcot-Marie-Tooth Disease, Axonal, Type 2f 27 0.046
101
FTD001 Foot Drop 33 0.046
102
BRC011 Brachial Plexus Neuropathy 36 0.045
103
c CHR534 Charcot-Marie-Tooth Disease, Type 1d 38 0.045
104
c CHR353 Charcot-Marie-Tooth Disease, Axonal, Type 2l 34 0.045
105
c CHR528 Charcot-Marie-Tooth Disease, Type 2j 32 0.043
106
c CHR529 Charcot-Marie-Tooth Disease, Type 2i 30 0.043
107
c CHR113 Charcot-Marie-Tooth Neuropathy Type 1 31 0.043
108
TBS001 Tabes Dorsalis 32 0.043
109
AMY003 Amyotrophic Neuralgia 27 0.042
110
c CHR313 Charcot-Marie-Tooth Neuropathy Type 4f 19 0.042
111
CNG102 Congenital Hypomyelination Neuropathy 18 0.042
112
c SNS009 Sensory Neuropathy Type 1 32 0.041