Search results for "junctional epidermolysis bullosa"

The MalaCard for "junctional epidermolysis bullosa" has been retired.
Searching MalaCards for entries containing "junctional epidermolysis bullosa"

210 hits were found for 'junctional epidermolysis bullosa'

# Family MCID Name MIFTS Score
1
EPD062 Epidermolysis Bullosa, Junctional, Non-Herlitz Type 41 14.054
2
EPD061 Epidermolysis Bullosa, Junctional, Herlitz Type 36 11.759
3
EPD045 Epidermolysis Bullosa, Junctional, with Pyloric Stenosis 37 9.603
4
P EPD025 Epidermolysis Bullosa with Pyloric Atresia 32 6.796
5
EPD032 Epidermolysis Bullosa, Late-Onset Localized Junctional, with Mental Retardation 15 5.189
6
CL1003 Col17a1-Related Junctional Epidermolysis Bullosa 7 4.374
7
LTN015 Late-Onset Junctional Epidermolysis Bullosa 13 3.897
8
LM3001 Lama3-Related Junctional Epidermolysis Bullosa 6 3.839
9
LMB026 Lamb3-Related Junctional Epidermolysis Bullosa 6 3.839
10
LMC001 Lamc2-Related Junctional Epidermolysis Bullosa 6 3.839
11
JNC002 Junctional Epidermolysis Bullosa Inversa 14 3.473
12
LCL021 Localized Junctional Epidermolysis Bullosa, Non-Herlitz Type 3 2.766
13
EPD016 Epidermolysis Bullosa 57 1.715
14
EPD006 Epidermolysis Bullosa Acquisita 45 0.673
15
P EPD003 Epidermolysis Bullosa Simplex 51 0.672
16
c RCS002 Recessive Dystrophic Epidermolysis Bullosa 52 0.641
17
P EPD009 Epidermolysis Bullosa Dystrophica 54 0.472
18
BLL006 Bullous Pemphigoid 58 0.276
19
P ESP024 Esophagitis 62 0.265
20
SKN016 Skin Disease 68 0.260
21
VSC012 Vesiculobullous Skin Disease 39 0.253
22
ADR038 Adermatoglyphia 48 0.228
23
P MSC005 Muscular Dystrophy 64 0.223
24
ALR002 Al-Raqad Syndrome 36 0.176
25
ESP023 Esophageal Disease 53 0.164
26
CNN005 Connective Tissue Disease 61 0.163
27
ESP021 Esophageal Cancer 75 0.162
28
CCT002 Cicatricial Pemphigoid 51 0.159
29
c EPD043 Epidermolysis Bullosa Dystrophica, Ad 21 0.158
30
P CLL015 Collagen Disease 49 0.154
31
P CRD011 Cardiomyopathy 67 0.144
32
P LRY019 Laryngitis 55 0.143
33
P LPS004 Lupus Erythematosus 63 0.133
34
HPT074 Hepatic Adenoma, Somatic 51 0.129
35
EPD040 Epidermolysis Bullosa Simplex with Pyloric Atresia 29 0.127
36
CRH001 Crohn's Disease 76 0.125
37
P APL006 Aplasia Cutis Congenita 48 0.124
38
AND005 Androgen Insensitivity Syndrome, Mild 16 0.121
39
DRM006 Dermatitis 61 0.119
40
PYL006 Pyloric Stenosis 46 0.119
41
HNM002 Hinman Syndrome 25 0.119
42
c DLT002 Dilated Cardiomyopathy 75 0.118
43
SKN027 Skin Conditions 45 0.117
44
P BRS047 Breast Cancer 100 0.116
45
P ART022 Arthritis 75 0.116
46
P HPT021 Hepatitis 70 0.116
47
KND001 Kindler Syndrome 50 0.113
48
P PNC044 Pancreatitis 60 0.112
49
PLV005 Pelviureteric Junction Obstruction 45 0.112
50
P PSR002 Psoriasis 63 0.110
51
DYS073 Dysphagia 49 0.108
52
ACD009 Acid-Labile Subunit, Deficiency of 48 0.107
53
P EPD002 Epidermolytic Hyperkeratosis 49 0.104
54
TRN023 Transient Bullous of the Newborn 25 0.102
55
CLT003 Colitis 59 0.101
56
NRM005 Neuromuscular Disease 57 0.101
57
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.099
58
P PNC035 Pancreatic Cancer 85 0.098
59
LRY022 Laryngoonychocutaneous Syndrome 26 0.095
60
ULC004 Ulcerative Colitis 75 0.093
61
P MYP004 Myopathy 67 0.093
62
c MCL062 Mucolipidosis Ii Alpha/beta 60 0.093
63
KRT009 Keratosis 50 0.092
64
P LYM118 Lymphoma 70 0.091
65
P THY032 Thyroiditis 54 0.090
66
P OST002 Osteoporosis 64 0.090
67
P DRM007 Dermatitis Herpetiformis 46 0.090
68
LNR006 Linear Iga Disease 41 0.090
69
P CTR002 Cataract 57 0.090
70
SRC014 Sarcoma 66 0.089
71
P HRP006 Herpes Simplex 65 0.085
72
P CNG001 Congenital Myasthenic Syndrome 53 0.085
73
c HPT001 Hepatitis C 68 0.084
74
PMP001 Pemphigus 49 0.084
75
ACR041 Acromelic Frontonasal Dysostosis 46 0.084
76
BRT030 Birth Defects 43 0.084
77
P ATX004 Ataxia 53 0.084
78
c MTR051 Maternal Uniparental Disomy of Chromosome 1 21 0.084
79
URT001 Urethritis 40 0.084
80
TNG009 Tongue Squamous Cell Carcinoma 74 0.084
81
NTR005 Nutritional Deficiency Disease 39 0.084
82
P MLT019 Multiple Myeloma 80 0.083
83
AND001 Anodontia 41 0.083
84
c ITG002 Itgb4-Related Epidermolysis Bullosa with Pyloric Atresia 5 0.083
85
CHL071 Child Syndrome 58 0.083
86
BLL007 Bullous Skin Disease 38 0.083
87
P GLM007 Glomerulonephritis 56 0.081
88
P LCH002 Lichen Planus 53 0.081
89
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 36 0.080
90
WLS001 Wilson Disease 72 0.079
91
PRT036 Peritonitis 62 0.079
92
CLN019 Colonic Disease 50 0.079
93
TBR010 Tuberculosis 69 0.076
94
P PNM007 Pneumonia 66 0.076
95
P PRD008 Periodontitis 46 0.076
96
MRF001 Marfan Syndrome 73 0.076
97
P PCH015 Pachyonychia Congenita 1 49 0.076
98
P AML002 Amelogenesis Imperfecta 43 0.076
99
KDS001 Kid Syndrome 53 0.075
100
PCK002 Pick Disease 67 0.072
101
c BSL007 Basal Cell Carcinoma 64 0.072
102
PHR003 Pharyngitis 58 0.072
103
P HMP007 Hemophilia 56 0.072
104
P CYS018 Cystitis 53 0.072
105
P ART084 Arteriovenous Fistula 44 0.072
106
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 30 0.072
107
P CTN003 Cutaneous Lupus Erythematosus 50 0.071
108
c PLN018 Peeling Skin Syndrome 2 35 0.071
109
WTH001 Withdrawal Disorder 41 0.070
110
P KRT005 Keratoacanthoma 45 0.069
111
DDN006 Duodenitis 44 0.069
112
c HMP029 Hemophilia a 64 0.067
113
PTR006 Peters Anomaly 64 0.067
114
P THL005 Thalassemia 61 0.067
115
P HRD011 Hereditary Spherocytosis 53 0.067
116
BRN106 Burns 52 0.067
117
ACT049 Acute Disseminated Encephalomyelitis 49 0.067
118
BLD053 Blood Platelet Disease 46 0.067
119
P BNG071 Benign Schwannoma 37 0.067
120
CHL069 Cholesteatoma 51 0.067
121
DWN001 Down Syndrome 65 0.066
122
PRD011 Proud Syndrome 42 0.066
123
c CNG031 Congenital Nervous System Abnormality 39 0.066
124
BNC003 Bone Cancer 45 0.066
125
P PMP005 Pemphigus Vulgaris 43 0.066
126
P RHM011 Rheumatoid Arthritis 88 0.066
127
P DRR001 Diarrhea 51 0.062
128
PRX075 Proximal Myopathy and Ophthalmoplegia 43 0.062
129
RDN001 Reading Disorder 39 0.062
130
HMC038 Hemochromatosis, Neonatal 27 0.062
131
P INF032 Infertility 61 0.061
132
GST078 Gastrointestinal Allergy 41 0.061
133
GST028 Gastric Squamous Cell Carcinoma 39 0.061
134
VSC006 Vascular Cancer 54 0.059
135
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.059
136
PSR001 Psoriatic Arthritis 64 0.057
137
P ENC018 Encephalopathy 59 0.057
138
PPL022 Papilloma 55 0.057
139
OCL020 Ocular Cicatricial Pemphigoid 52 0.057
140
c INF067 Inflammatory Bowel Disease 10 51 0.057
141
HYP457 Hypertrophic Scars 45 0.057
142
PRT019 Protein-Losing Enteropathy 41 0.057
143
P HYP009 Hypertrophic Pyloric Stenosis 41 0.057
144
ECT005 Ectropion 40 0.057
145
DDN011 Duodenal Atresia 39 0.057
146
c CHR579 Chiari Malformation Type Ii 38 0.057
147
ADP007 Adie Pupil 34 0.057
148
URT037 Urethral Stricture 33 0.057
149
c ACT072 Acute Laryngitis 30 0.057
150
c CHR020 Chronic Interstitial Cystitis 41 0.056
151
AND015 Androgen Insensitivity 63 0.049
152
RSP006 Respiratory System Disease 62 0.049
153
P RHN004 Rhinitis 61 0.049
154
ALL010 Allergic Contact Dermatitis 57 0.049
155
P EMR001 Emery-Dreifuss Muscular Dystrophy 53 0.049
156
ECT006 Ectodermal Dysplasia 47 0.049
157
SPC010 Speech and Communication Disorders 46 0.049
158
HMN009 Hemangioblastoma 45 0.049
159
THR035 Thrombasthenia 42 0.049
160
P HMF004 Hemifacial Spasm 39 0.049
161
BWN006 Bowen's Disease 31 0.049
162
P OST012 Osteoarthritis 82 0.044
163
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 76 0.044
164
P ALP004 Alport Syndrome 68 0.044
165
P PLM036 Pulmonary Fibrosis 68 0.044
166
CHR012 Chronic Granulomatous Disease 65 0.044
167
ALL003 Allergic Rhinitis 64 0.044
168
DMN002 Dementia 64 0.044
169
GLN010 Glanzmann Thrombasthenia 63 0.044
170
P ANR007 Anorexia Nervosa 63 0.044
171
P ATP001 Atopic Dermatitis 62 0.044
172
LSH001 Leishmaniasis 62 0.044
173
P HMN010 Hemangioma 60 0.044
174
ETN001 Eating Disorder 60 0.044
175
INT066 Interstitial Lung Disease 58 0.044
176
LYM022 Lymphangioma 54 0.044
177
P INT063 Intellectual Disability 53 0.044
178
KLD001 Keloids 51 0.044
179
RHM028 Rheumatic Heart Disease 51 0.044
180
INT051 Intussusception 50 0.044
181
HMG005 Hemoglobinopathy 50 0.044
182
LMB062 Limb Ischemia 48 0.044
183
CRD118 Cardiovascular Cancer 47 0.044
184
FRM003 Farmer's Lung 47 0.044
185
P CNN004 Connective Tissue Cancer 45 0.044
186
HDN002 Head Injury 45 0.044
187
LMB050 Limbal Stem Cell Deficiency 45 0.044
188
PHY002 Physical Disorder 44 0.044
189
DSC009 Discoid Lupus Erythematosus 44 0.044
190
GLS007 Glossitis 44 0.044
191
P ICH001 Ichthyosis Vulgaris 44 0.044
192
SPN032 Spindle Cell Carcinoma 43 0.044
193
ANH002 Anhidrosis 42 0.044
194
PLM029 Palmoplantar Keratosis 42 0.044
195
BCK006 Back Pain 42 0.044
196
BSL006 Basaloid Squamous Cell Carcinoma 41 0.044
197
CRN025 Corneal Dystrophy 41 0.044
198
CDS002 Codas Syndrome 40 0.044
199
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 37 0.044
200
PLM136 Palmoplantar Keratoderma, Nonepidermolytic 37 0.044
201
MSN004 Mesenchymal Cell Neoplasm 36 0.044
202
P GLM006 Glomangioma 34 0.044
203
CHR463 Chronic Actinic Dermatitis 33 0.044
204
ATM016 Autoimmune Disease of Skin and Connective Tissue 31 0.044
205
LCH013 Lichen Planus Pemphigoides 30 0.044
206
SCP009 Scapuloperoneal Myopathy, X-Linked Dominant 29 0.044
207
BNG033 Benign Perivascular Tumor 28 0.044
208
CRD007 Cardiovascular Organ Benign Neoplasm 27 0.044
209
P HYP658 Hypoplastic Amelogenesis Imperfecta 27 0.044
210
P EMR004 Emery-Dreifuss Muscular Dystrophy, X-Linked 22 0.044