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"

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

# Family MCID Name MIFTS Score
1
CRN246 Cranioosteoarthropathy 31 6.398
2
c HYP533 Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 25 6.053
3
P PRM018 Primary Hypertrophic Osteoarthropathy 39 0.323
4
P NRP001 Neuropathy 60 0.196
5
P HRT032 Heart Disease 76 0.186
6
TTR016 Tetra-Amelia Syndrome 36 0.179
7
END072 Endotheliitis 42 0.175
8
P ADN016 Adenocarcinoma 69 0.154
9
P PLM037 Pulmonary Hypertension 79 0.137
10
P ART022 Arthritis 75 0.136
11
P MSC007 Muscle Hypertrophy 59 0.128
12
SRC014 Sarcoma 66 0.128
13
P MYL005 Myelofibrosis 67 0.123
14
P LKM002 Leukemia 70 0.114
15
TTH006 Tooth Disease 52 0.112
16
P ESP024 Esophagitis 62 0.112
17
PRS047 Prostatitis 56 0.110
18
PRS037 Periostitis 30 0.107
19
P ART023 Arthropathy 63 0.104
20
P LNG032 Lung Cancer 94 0.099
21
P CRV039 Cervicitis 44 0.096
22
P LPS004 Lupus Erythematosus 63 0.092
23
P CHR071 Charcot-Marie-Tooth Disease 66 0.090
24
NPH003 Nephrocalcinosis 46 0.085
25
VSC011 Vasculitis 62 0.085
26
P LRY019 Laryngitis 55 0.084
27
P PLY019 Polyneuropathy 54 0.084
28
TBR010 Tuberculosis 69 0.081
29
P PNM007 Pneumonia 66 0.080
30
OST017 Osteomyelitis 59 0.077
31
LVR012 Liver Cirrhosis 67 0.076
32
BRT030 Birth Defects 43 0.076
33
ACR041 Acromelic Frontonasal Dysostosis 46 0.076
34
P PTS002 Ptosis 56 0.073
35
P AGM001 Agammaglobulinemia 64 0.072
36
MYX004 Myxedema 38 0.069
37
NRM005 Neuromuscular Disease 57 0.069
38
P PNC001 Pancytopenia 52 0.066
39
ACN002 Acanthosis Nigricans 57 0.065
40
c SYS001 Systemic Lupus Erythematosus 87 0.065
41
P PRP019 Peripheral Nervous System Disease 54 0.064
42
ADR038 Adermatoglyphia 48 0.064
43
CRH001 Crohn's Disease 76 0.062
44
P CHR102 Charcot-Marie-Tooth Neuropathy 43 0.062
45
OTT002 Otitis Media 66 0.062
46
NRT004 Neuritis 52 0.062
47
P HMN036 Hemangiopericytoma, Malignant 44 0.061
48
PLN005 Palindromic Rheumatism 43 0.060
49
ESP021 Esophageal Cancer 75 0.060
50
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 36 0.060
51
c THR092 Thrombophilia Due to Thrombin Defect 56 0.059
52
c CHR536 Charcot-Marie-Tooth Disease, Type 1a 56 0.055
53
NRP015 Neuropathy, Congenital Hypomyelinating 56 0.055
54
c CHR532 Charcot-Marie-Tooth Disease, Type 2e 47 0.054
55
c HRD088 Hereditary Neuropathies 41 0.053
56
c CHR527 Charcot-Marie-Tooth Disease, Type 1b 51 0.053
57
PLM001 Pulmonary Tuberculosis 68 0.052
58
c CHR407 Charcot-Marie-Tooth Disease, Type 4f 38 0.051
59
c CHR520 Charcot-Marie-Tooth Disease, Axonal, Type 2s 36 0.050
60
PLM017 Pulmonary Alveolar Microlithiasis 46 0.049
61
P RNL059 Renal-Hepatic-Pancreatic Dysplasia 35 0.049
62
c SPN225 Spondyloarthropathy 1 63 0.048
63
NRL005 Neurilemmoma 51 0.046
64
SNS003 Sensory Peripheral Neuropathy 47 0.046
65
GLL022 Guillain-Barre Syndrome 56 0.044
66
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 32 0.043
67
c LNG031 Lung Benign Neoplasm 44 0.042
68
HMP018 Hemophilic Arthropathy 36 0.042