Search results for "hemoglobin c - beta-thalassemia"

The MalaCard for "hemoglobin c - beta-thalassemia" has been retired.
Searching MalaCards for entries containing "hemoglobin c - beta-thalassemia"

399 hits were found for 'hemoglobin c - beta-thalassemia'

# Family MCID Name MIFTS Score
1
c HMG001 Hemoglobin C Disease 46 6.265
2
SCK003 Sickle Cell Anemia 72 3.421
3
c HPT003 Hepatitis a 55 0.227
4
c VRL010 Viral Hepatitis 60 0.226
5
P BRS047 Breast Cancer 100 0.196
6
c HPT016 Hepatitis B 61 0.191
7
P NRB001 Neuroblastoma 70 0.165
8
NRN002 Neuronitis 40 0.163
9
P PRS040 Prostate Cancer 89 0.152
10
PRS047 Prostatitis 56 0.150
11
HMG012 Hemoglobin Constant Spring 18 0.148
12
P MYC007 Myocardial Infarction 80 0.140
13
P OBS005 Obesity 91 0.139
14
P CLR023 Colorectal Cancer 96 0.131
15
P LNG032 Lung Cancer 92 0.130
16
CSY001 C Syndrome 49 0.128
17
P HRT032 Heart Disease 64 0.126
18
RTN023 Retinitis 49 0.126
19
HV1006 Hiv-1 80 0.125
20
HMG025 Hemoglobin H Disease, Nondeletional 36 0.123
21
ATH003 Atherosclerosis 63 0.122
22
P CRN211 Coronary Artery Disease 74 0.121
23
P ADN016 Adenocarcinoma 69 0.120
24
HYP266 Hypoxia 55 0.119
25
MLN008 Melanoma 61 0.118
26
ART111 Artery Disease 56 0.117
27
LVR012 Liver Cirrhosis 71 0.115
28
GST053 Gastric Cancer 52 0.110
29
P HYP607 Hypercholesterolemia, Familial 77 0.107
30
c ACT075 Acute Myocardial Infarction 61 0.103
31
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.100
32
ACQ007 Acquired Immunodeficiency Syndrome 60 0.100
33
HMN014 Human Immunodeficiency Virus Infectious Disease 46 0.099
34
PRT036 Peritonitis 65 0.099
35
P RNL014 Renal Cell Carcinoma 80 0.098
36
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.097
37
P ESP024 Esophagitis 62 0.096
38
c BLD124 Bleeding Disorder, Platelet-Type, 11 37 0.096
39
P URF003 Urofacial Syndrome 1 51 0.094
40
HMG009 Hemoglobin Zurich 15 0.092
41
P MTH007 Methemoglobinemia 44 0.092
42
GLC008 Glucose Metabolism Disease 44 0.091
43
P CRV039 Cervicitis 45 0.091
44
TBR010 Tuberculosis 70 0.089
45
MDY003 Mody, Type Ii 36 0.089
46
LPD008 Lipid Metabolism Disorder 42 0.087
47
IMP003 Impaired Renal Function Disease 36 0.086
48
P NRP001 Neuropathy 57 0.086
49
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.086
50
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 25 0.085
51
P HMG016 Hemoglobin Sd 19 0.084
52
VSC007 Vascular Disease 51 0.084
53
P OVR042 Ovarian Cancer 73 0.082
54
GST033 Gestational Diabetes 54 0.081
55
P GLB002 Glioblastoma 65 0.081
56
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 59 0.081
57
HYP066 Hyperglycemia 61 0.080
58
SRC014 Sarcoma 66 0.079
59
c CLD010 Cold-Induced Sweating Syndrome 1 43 0.078
60
P MYL007 Myeloma 52 0.077
61
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 21 0.077
62
HPT074 Hepatic Adenoma, Somatic 35 0.077
63
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 41 0.076
64
ISC006 Ischemic Heart Disease 54 0.076
65
SXL003 Sexual Disorder 45 0.075
66
PRP027 Peripheral Vascular Disease 69 0.075
67
HYP056 Hypoglycemia 60 0.073
68
HMG002 Hemoglobinuria 49 0.072
69
P PLY018 Polycythemia 58 0.072
70
PLM033 Pulmonary Embolism 59 0.072
71
c MLT019 Multiple Myeloma 77 0.070
72
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 45 0.070
73
c PND001 Pain Disorder 53 0.070
74
ANG054 Angina Pectoris 48 0.070
75
P HYP086 Hypothyroidism 63 0.070
76
ANM029 Anemia, Sideroblastic, X-Linked 53 0.069
77
c MCL042 Macular Degeneration, Age-Related, 1 71 0.069
78
P PLY011 Polycystic Ovary Syndrome 64 0.068
79
P AST005 Asthma 80 0.068
80
P NTR004 Neutropenia 59 0.068
81
c THR092 Thrombophilia Due to Thrombin Defect 56 0.067
82
P DRR001 Diarrhea 60 0.067
83
DMN002 Dementia 62 0.067
84
URN009 Urinary System Disease 52 0.066
85
P LYM026 Lymphoblastic Leukemia 60 0.066
86
P MYP004 Myopathy 67 0.066
87
c MCR129 Microvascular Complications of Diabetes 1 55 0.066
88
TRN018 Transitional Cell Carcinoma 56 0.065
89
PRD007 Periodontal Disease 42 0.065
90
DNG002 Dengue Hemorrhagic Fever 60 0.065
91
IMM071 Immunodeficiency 12 27 0.065
92
P END044 Endometriosis 53 0.065
93
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 77 0.065
94
c CHR090 Chronic Lymphocytic Leukemia 73 0.064
95
P NSP012 Nasopharyngeal Carcinoma 59 0.064
96
P ESS003 Essential Thrombocythemia 66 0.064
97
HMT002 Hematologic Cancer 62 0.064
98
PRT014 Protein S Deficiency 54 0.064
99
P PLM036 Pulmonary Fibrosis 69 0.064
100
P GT001 Gout 58 0.063
101
CLT003 Colitis 56 0.063
102
P HYP060 Hyperinsulinism 58 0.063
103
LNG099 Lung Disease 63 0.062
104
RSP002 Respiratory Syncytial Virus Infectious Disease 31 0.062
105
VTM003 Vitamin Metabolic Disorder 31 0.061
106
GLC006 Galactosemia 64 0.061
107
IMM076 Immunodeficiency 24 27 0.060
108
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 45 0.060
109
BRN004 Brain Edema 51 0.059
110
LRN003 Learning Disability 49 0.059
111
HPY002 H. Pylori Infection 58 0.059
112
c CRN174 Coronary Heart Disease 2 19 0.058
113
CHR005 Chorioamnionitis 47 0.058
114
STR067 Stroke, Ischemic 74 0.058
115
DNG003 Dengue Disease 60 0.058
116
P SKN013 Skin Benign Neoplasm 38 0.058
117
ALP014 Alpha-Thalassemia/mental Retardation Syndrome 54 0.058
118
HYD038 Hydrops Fetalis, Nonimmune 39 0.058
119
PLS007 Plasmodium Falciparum Malaria 56 0.058
120
ATM052 Autoimmune Disease 1 26 0.057
121
PHR003 Pharyngitis 58 0.057
122
DBT084 Diabetes Mellitus, Ketosis-Prone 28 0.057
123
P CLR108 Colorectal Adenoma 60 0.056
124
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 35 0.056
125
P DMY001 Demyelinating Polyneuropathy 41 0.056
126
OST017 Osteomyelitis 60 0.056
127
CHL067 Cholecystitis 57 0.056
128
CHR008 Choroiditis 43 0.056
129
GLC003 Glucose Intolerance 56 0.055
130
P FML035 Familial Hyperlipidemia 49 0.055
131
P ALC004 Alcohol Abuse 57 0.055
132
ADL002 Adult Syndrome 53 0.054
133
c TRC078 Trichohepatoenteric Syndrome 2 30 0.054
134
PPL022 Papilloma 54 0.054
135
P EXN002 Exanthem 57 0.054
136
BRN106 Burns 52 0.054
137
P HYP069 Hyperparathyroidism 57 0.054
138
ATM053 Autoimmune Disease 2 16 0.054
139
P ENC004 Encephalitis 60 0.054
140
P CNJ013 Conjunctivitis 65 0.053
141
P HYP071 Hypersensitivity Reaction Type Ii Disease 46 0.053
142
SPN051 Spondylitis 50 0.053
143
PLC008 Placenta Disease 33 0.053
144
P PLY019 Polyneuropathy 53 0.053
145
PNC041 Pancreatic Ductal Adenocarcinoma 64 0.053
146
MLT021 Multiple System Atrophy 71 0.053
147
ATN002 Autonomic Nervous System Disease 46 0.052
148
P HYP076 Hyperthyroidism 59 0.052
149
KWS001 Kwashiorkor 45 0.052
150
P SYP003 Syphilis 51 0.052
151
RDN001 Reading Disorder 39 0.051
152
NNL002 Nonalcoholic Steatohepatitis 49 0.051
153
P SDD001 Sudden Infant Death Syndrome 60 0.051
154
ATM014 Autoimmune Disease of Endocrine System 37 0.051
155
CYN002 Cyanosis, Transient Neonatal 29 0.051
156
P ECL001 Eclampsia 55 0.051
157
CRV038 Cervical Squamous Cell Carcinoma 58 0.051
158
HNZ001 Heinz Body Anemia 40 0.050
159
P GST044 Gastritis 64 0.050
160
c PRC016 Pre-Eclampsia 57 0.050
161
BRN071 Brain Injury 51 0.050
162
LYM019 Lymphosarcoma 52 0.050
163
ACD009 Acid-Labile Subunit, Deficiency of 37 0.050
164
P PLY014 Polycystic Kidney Disease 60 0.050
165
P HYP117 Hypertriglyceridemia 65 0.049
166
P THY097 Thyroid Hormone Resistance 54 0.049
167
RHM001 Rheumatic Fever 50 0.049
168
INT002 Intermittent Claudication 56 0.049
169
RFR010 Refractory Anemia 43 0.049
170
c MYC058 Myocardial Infarction 2 28 0.049
171
AML029 Ameloblastoma 49 0.049
172
SYS003 Systolic Heart Failure 42 0.048
173
DCH001 Duchenne Muscular Dystrophy 81 0.048
174
MLD001 Melioidosis 67 0.048
175
SCH014 Schistosomiasis 59 0.048
176
TXC005 Toxic Shock Syndrome 61 0.048
177
HDN004 Head and Neck Carcinoma 54 0.048
178
SHW002 Shwachman-Diamond Syndrome 59 0.048
179
P EPD002 Epidermolytic Hyperkeratosis 51 0.047
180
c GRV008 Graves Disease 1 44 0.047
181
ATM012 Autoimmune Disease of Blood 36 0.047
182
LMB062 Limb Ischemia 48 0.047
183
BNF002 Bone Fracture 46 0.047
184
c THR037 Thrombocytopenia 2 36 0.047
185
CRV047 Cervical Cancer, Somatic 65 0.047
186
P LCT001 Lactic Acidosis 52 0.047
187
BRN080 Brain Ischemia 42 0.047
188
P MYL005 Myelofibrosis 67 0.047
189
P PCH001 Pachyonychia Congenita 54 0.047
190
APH001 Aphthous Stomatitis 62 0.047
191
GTR002 Goiter 54 0.047
192
CHL069 Cholesteatoma 51 0.047
193
THY030 Thyroid Gland Disease 52 0.047
194
c DBT040 Diabetes Mellitus, Insulin-Dependent, 2 26 0.046
195
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 59 0.046
196
MLT075 Multifocal Motor Neuropathy 40 0.046
197
GRN017 Granulocytopenia 39 0.046
198
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 30 0.046
199
P RTN014 Retinal Artery Occlusion 32 0.046
200
PLS009 Plasma Cell Neoplasm 47 0.046
201
GNG011 Gingival Disease 50 0.045
202
P LPR003 Leprosy 70 0.045
203
LSH001 Leishmaniasis 63 0.045
204
SPT004 Septic Arthritis 60 0.045
205
P NRV006 Nervous System Cancer 62 0.045
206
TTH006 Tooth Disease 52 0.045
207
P CRT072 Creutzfeldt-Jakob Disease 62 0.045
208
ATR060 Atrial Standstill, Digenic 51 0.045
209
INS001 Insulinoma 60 0.045
210
DBT010 Diabetic Neuropathy 55 0.045
211
CRB025 Carbohydrate Metabolic Disorder 46 0.045
212
ATM055 Autoimmune Disease 4 16 0.045
213
P RSP003 Respiratory Failure 68 0.044
214
P BPL003 Bipolar Disorder 58 0.044
215
P LNG064 Lung Cancer Susceptibility 3 62 0.044
216
STM007 Stomatitis 50 0.044
217
c ADL001 Adult Lymphoma 40 0.044
218
CRZ001 Crouzon Syndrome 70 0.044
219
BRN118 Brain Small Vessel Disease with or Without Ocular Anomalies 42 0.044
220
PRT038 Protein-Energy Malnutrition 48 0.044
221
CRT015 Carotid Artery Occlusion 43 0.044
222
ANM001 Anemia of Prematurity 44 0.043
223
ALC007 Alcohol Dependence 66 0.043
224
CHL028 Childhood Type Dermatomyositis 40 0.043
225
BCL002 B Cell Deficiency 50 0.043
226
c DRR009 Diarrhea 6 30 0.043
227
VRR004 Verrucous Carcinoma 54 0.043
228
RNL101 Renal Cell Carcinoma, Papillary 63 0.042
229
P LFR001 Li-Fraumeni Syndrome 79 0.042
230
BRS051 Breast Disease 57 0.042
231
VSC006 Vascular Cancer 51 0.042
232
FML039 Female Reproductive System Disease 49 0.042
233
KRT002 Keratomalacia 50 0.041
234
BRC012 Brucellosis 66 0.041
235
c CHR418 Chronic Leukemia 48 0.041
236
CRB004 Cerebral Artery Occlusion 39 0.041
237
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 36 0.041
238
PLM014 Pleomorphic Adenoma 51 0.041
239
P PYL005 Pyelonephritis 52 0.041
240
CRT049 Critical Limb Ischemia 51 0.041
241
GLC009 Glucosephosphate Dehydrogenase Deficiency 38 0.041
242
MSC004 Muscle Tissue Disease 35 0.041
243
ICH002 Ichthyosis Bullosa of Siemens 44 0.040
244
PLM102 Palmoplantar Keratoderma, Epidermolytic 46 0.040
245
EPD047 Epidermolysis Bullosa Simplex, Koebner Type 37 0.040
246
DCB001 Decubitus Ulcer 44 0.040
247
KRT009 Keratosis 50 0.040
248
OST032 Osteofibrous Dysplasia 39 0.040
249
c HYP595 Hypertension, Essential 69 0.040
250
c THR048 Thrombocytopenia 4 29 0.040
251
P MSC033 Muscle Disorders 52 0.040
252
P AGG001 Aggressive Periodontitis 49 0.040
253
TRM010 Traumatic Brain Injury 52 0.040
254
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 28 0.039
255
c ACT071 Acute Kidney Failure 48 0.039
256
ATN005 Autonomic Dysfunction 44 0.039
257
CRB085 Cerebral Hemorrhage 40 0.039
258
MND006 Mondor Disease 20 0.039
259
SPN209 Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations 45 0.039
260
EPD028 Epidermolysis Bullosa Simplex, Dowling-Meara Type 41 0.039
261
GST028 Gastric Squamous Cell Carcinoma 39 0.039
262
c CNT028 Central Retinal Artery Occlusion 34 0.039
263
c ACT042 Acute Pyelonephritis 47 0.039
264
HYP029 Hyperthyroxinemia 25 0.039
265
TRN015 Transient Cerebral Ischemia 57 0.038
266
CRV040 Cervix Carcinoma 50 0.038
267
CRN030 Coronary Stenosis 50 0.038
268
MDY005 Mody, Type I 31 0.037
269
HML006 Hemolytic Anemia Due to G6pd Deficiency 31 0.037
270
c CHR283 Chronic Inflammatory Demyelinating Polyneuropathy 38 0.037
271
PRP021 Peripheral Nervous System Neoplasm 49 0.037
272
URM002 Uremia 36 0.037
273
SNS023 Sensory System Cancer 45 0.037
274
OCL069 Ocular Motor Apraxia 44 0.037
275
DHY014 Dehydrated Hereditary Stomatocytosis with or Without Pseudohyperkalemia and/or Perinatal Edema 25 0.037
276
P EPD003 Epidermolysis Bullosa Simplex 50 0.037
277
RHM029 Rheumatic Fever-Related Antigen Rheumatic Fever, Acute, Susceptibility to, Included 24 0.037
278
MRS001 Marasmus 39 0.037
279
DYS015 Dysentery 42 0.037
280
P MRC003 Mercury Poisoning 38 0.037
281
ETH004 Euthyroid Sick Syndrome 37 0.037
282
TST018 Testicular Yolk Sac Tumor 40 0.037
283
CHR100 Chronic Ulcer of Skin 32 0.037
284
c DBT056 Diabetes Mellitus, Insulin-Dependent, 4 19 0.037
285
BSL006 Basaloid Squamous Cell Carcinoma 40 0.037
286
c MLG080 Malignant Secondary Hypertension 28 0.037
287
HRN022 Hearing Loss/deafness 23 0.037
288
TXC004 Toxic Diffuse Goiter 21 0.037
289
P DYS070 Dysalbuminemic Hyperthyroxinemia 22 0.037
290
PRM123 Paramyloidosis 17 0.037
291
FRB001 Farber Lipogranulomatosis 54 0.036
292
c MSC113 Muscular Dystrophy, Limb-Girdle, Type 2b 39 0.036
293
CRN017 Coronary Thrombosis 46 0.036
294
P ATR005 Atrophic Gastritis 47 0.036
295
ALX002 Alexithymia 37 0.036
296
P TRC086 Trichohepatoenteric Syndrome 1 46 0.035
297
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 45 0.035
298
INT007 Intermediate Coronary Syndrome 52 0.035
299
FML038 Female Reproductive Organ Cancer 50 0.035
300
GRW007 Growth Hormone Deficiency 49 0.035
301
SDD007 Sudden Cardiac Death 46 0.035
302
SND007 Sandhoff Disease, Infantile, Juvenile, and Adult Forms 58 0.034
303
P ICH001 Ichthyosis Vulgaris 44 0.034
304
P SLL003 Salla Disease 44 0.034
305
STT007 Steatocystoma Multiplex 45 0.034
306
c DYS168 Dyserythropoietic Anemia, Congenital, Type Iv 25 0.034
307
c DMN006 Diamond-Blackfan Anemia 3 29 0.034
308
EPD041 Epidermolysis Bullosa Simplex, Weber-Cockayne Type 38 0.034
309
ICH036 Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis 29 0.034
310
P PRM001 Primary Cutaneous Amyloidosis 54 0.034
311
ANM030 Anemia, Hypochromic Microcytic 37 0.034
312
CRN036 Craniopharyngioma 54 0.034
313
c EPD058 Epidermolysis Bullosa Simplex, Recessive 1 28 0.034
314
c DFN280 Deafness, Autosomal Recessive 31 0.034
315
c DBT082 Diabetes Mellitus, Insulin-Dependent, 12 23 0.034
316
OSG001 Osgood-Schlatter's Disease 32 0.034
317
VLV044 Vulvar Intraepithelial Neoplasia 44 0.034
318
ODN006 Odontoma 34 0.034
319
BRN028 Brain Cancer 69 0.034
320
P CLC005 Celiac Disease 67 0.034
321
P SZR006 Seizure Disorder 56 0.034
322
PLM129 Pulmonary Disease, Chronic Obstructive 61 0.034
323
P SHR029 Short Syndrome 60 0.034
324
P MTC069 Mitochondrial Disorders 51 0.034
325
P HMR012 Hemorrhagic Fever 55 0.034
326
CRV069 Cervix Disease 31 0.034
327
LYM067 Lymphoid Leukemia 38 0.034
328
SYN036 Syncope 45 0.034
329
MNT045 Montefiore Syndrome 11 0.034
330
P RCK004 Rickets 59 0.033
331
VSC003 Visceral Leishmaniasis 56 0.033
332
ORL004 Oral Submucous Fibrosis 52 0.033
333
AYM001 Ayme-Gripp Syndrome 40 0.033
334
VSC002 Vascular Dementia 41 0.033
335
HLL004 Hellp Syndrome 48 0.033
336
URN003 Urinary Schistosomiasis 49 0.033
337
PRT082 Preterm Premature Rupture of the Membranes 46 0.033
338
FML037 Female Breast Cancer 49 0.033
339
CRD137 Cardiogenic Shock 44 0.033
340
PRP083 Porphyria, Acute Intermittent 54 0.032
341
ACH005 Achalasia 55 0.032
342
NSP001 Nasopharynx Carcinoma 54 0.032
343
NSD001 Nose Disease 51 0.032
344
LPR001 Lepromatous Leprosy 50 0.032
345
c AST037 Asthma 1 35 0.032
346
GLS001 Gliosarcoma 54 0.032
347
c LKM004 Leukemia, B-Cell, Chronic 24 0.032
348
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 21 0.032
349
DBT008 Diabetic Angiopathy 30 0.032
350
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 44 0.032
351
ESN011 Eisenmenger Syndrome 45 0.032
352
SPN185 Spinal Cord Infarction 36 0.032
353
c ACT004 Acute Diarrhea 38 0.032
354
RTN003 Retinal Ischemia 48 0.032
355
c ART106 Arterial Calcification, Generalized, of Infancy, 1 32 0.030
356
BRN056 Bronchopulmonary Dysplasia 56 0.030
357
VTM001 Vitamin K Deficiency Hemorrhagic Disease 37 0.030
358
VSC009 Vascular Skin Disease 21 0.030
359
PRD004 Prediabetes Syndrome 40 0.030
360
c CHR546 Chronic Mountain Sickness 42 0.030
361
FRN014 Fournier Gangrene 33 0.030
362
NSP003 Nasopharyngeal Disease 25 0.030
363
ACT056 Acute Cor Pulmonale 29 0.030
364
FNT004 Fainting 33 0.030
365
ATM013 Autoimmune Disease of Cardiovascular System 14 0.030
366
FTL021 Fetal Macrosomia 38 0.030
367
P DYS007 Dyskeratosis Congenita 64 0.028
368
MDY006 Mody, Type Iv 31 0.028
369
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 35 0.028
370
c DBT034 Diabetes Mellitus, Insulin-Dependent, 20 24 0.028
371
PST095 Post-Thrombotic Syndrome 48 0.028
372
CPL005 Capillary Disease 39 0.028
373
MTC005 Mitochondrial Metabolism Disease 37 0.028
374
PHM001 Phimosis 32 0.028
375
DBT062 Diabetic Foot Ulcers 55 0.028
376
FNC002 Functional Diarrhea 39 0.028
377
ORL014 Oral Pharyngeal Disorders 13 0.028
378
PLY125 Polycythemia Vera, Somatic 63 0.026
379
PRL019 Prolidase Deficiency 39 0.026
380
P ERY048 Erythrocytosis, Familial, 2 42 0.026
381
c THR103 Thrombocytopenia, Congenital Amegakaryocytic 45 0.026
382
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 36 0.026
383
P EXP004 Exophthalmos 56 0.026
384
IMM070 Immunodeficiency 13 30 0.026
385
HML021 Hemolytic Anemia, Nonspherocytic, Due to Glucose Phosphate Isomerase Deficiency 23 0.026
386
TWN001 Twin-to-Twin Transfusion Syndrome 47 0.026
387
c DMN028 Diamond-Blackfan Anemia 12 27 0.026
388
LGD001 Leg Dermatosis 17 0.026
389
P AVS004 Avascular Necrosis of the Femoral Head 55 0.026
390
MCR017 Macrocytic Anemia 43 0.026
391
ALB002 Albinism 43 0.026
392
PRC003 Proctitis 42 0.026
393
ULC005 Ulcer of Lower Limbs 21 0.026
394
PRS036 Parasitic Protozoa Infectious Disease 45 0.026
395
SBC016 Subacute Delirium 23 0.026
396
KTT001 Ketothiolase Deficiency 26 0.026
397
c DBT059 Diabetes Mellitus, Insulin-Dependent, 8 18 0.026
398
GGN002 Gigantism 29 0.026
399
PRX034 Peroxisome Disorders 24 0.026