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"

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

# Family MCID Name MIFTS Score
1
CRN246 Cranioosteoarthropathy 32 6.451
2
c HYP533 Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 22 6.081
3
P PRM018 Primary Hypertrophic Osteoarthropathy 39 0.330
4
P NRP001 Neuropathy 57 0.217
5
P HRT032 Heart Disease 64 0.192
6
END072 Endotheliitis 41 0.183
7
c CNG401 Congenital Heart Disease 67 0.170
8
HPT074 Hepatic Adenoma, Somatic 35 0.165
9
P ADN016 Adenocarcinoma 69 0.155
10
P PLM037 Pulmonary Hypertension 78 0.144
11
P MYL005 Myelofibrosis 67 0.133
12
TTH006 Tooth Disease 52 0.130
13
SRC014 Sarcoma 66 0.128
14
P MSC007 Muscle Hypertrophy 55 0.127
15
P LKM002 Leukemia 70 0.116
16
PRS037 Periostitis 31 0.115
17
P ESP024 Esophagitis 62 0.112
18
P CHR071 Charcot-Marie-Tooth Disease 66 0.109
19
PRS047 Prostatitis 56 0.109
20
c CLD010 Cold-Induced Sweating Syndrome 1 43 0.105
21
P ART023 Arthropathy 63 0.104
22
P PLY019 Polyneuropathy 53 0.101
23
P CRV039 Cervicitis 45 0.097
24
P LNG032 Lung Cancer 92 0.095
25
P LPS004 Lupus Erythematosus 63 0.093
26
NPH003 Nephrocalcinosis 47 0.091
27
VSC011 Vasculitis 62 0.089
28
P PNM007 Pneumonia 67 0.088
29
P LRY019 Laryngitis 55 0.086
30
P PTS002 Ptosis 56 0.086
31
LVR012 Liver Cirrhosis 71 0.083
32
P CHR102 Charcot-Marie-Tooth Neuropathy 43 0.083
33
OST017 Osteomyelitis 60 0.083
34
TBR010 Tuberculosis 70 0.082
35
PRP019 Peripheral Nervous System Disease 52 0.081
36
NRM005 Neuromuscular Disease 56 0.081
37
NRT004 Neuritis 52 0.076
38
PLN005 Palindromic Rheumatism 43 0.076
39
BRT030 Birth Defects 44 0.076
40
ACN002 Acanthosis Nigricans 59 0.076
41
P PNC001 Pancytopenia 53 0.073
42
P AGM001 Agammaglobulinemia 63 0.072
43
ACR041 Acromelic Frontonasal Dysostosis 45 0.071
44
EPT020 Epithelioid Hemangioendothelioma 46 0.070
45
c THR092 Thrombophilia Due to Thrombin Defect 56 0.068
46
c SPN225 Spondyloarthropathy 1 62 0.067
47
c CHR536 Charcot-Marie-Tooth Disease, Type 1a 55 0.066
48
c CHR532 Charcot-Marie-Tooth Disease, Type 2e 45 0.066
49
c SYS001 Systemic Lupus Erythematosus 87 0.066
50
c HRD088 Hereditary Neuropathies 35 0.065
51
SNS003 Sensory Peripheral Neuropathy 44 0.065
52
c CHR527 Charcot-Marie-Tooth Disease, Type 1b 48 0.065
53
CRH001 Crohn's Disease 76 0.064
54
P RNL059 Renal-Hepatic-Pancreatic Dysplasia 39 0.064
55
OTT002 Otitis Media 66 0.063
56
ADR038 Adermatoglyphia 39 0.063
57
ESP021 Esophageal Cancer 75 0.061
58
GLL022 Guillain-Barre Syndrome 58 0.061
59
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 34 0.060
60
HMP018 Hemophilic Arthropathy 34 0.059
61
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 32 0.057
62
PLM001 Pulmonary Tuberculosis 69 0.054
63
PLM017 Pulmonary Alveolar Microlithiasis 46 0.053