Search results for "hemihypertrophy"

The MalaCard for "hemihypertrophy" has been retired.
Searching MalaCards for entries containing "hemihypertrophy"

321 hits were found for 'hemihypertrophy'

# Family MCID Name MIFTS Score
1
HYP524 Hypoinsulinemic Hypoglycemia with Hemihypertrophy 13 5.262
2
PRT093 Proteus Syndrome, Somatic 55 4.693
3
HYP493 Hypoinsulinemic Hypoglycemia and Body Hemihypertrophy 4 2.376
4
HMH001 Hemihypertrophy Intestinal Web Corneal Opacity 3 2.376
5
ISL101 Isolated Hemihyperplasia 25 2.353
6
MCR030 Macrocephaly Mesodermal Hamartoma Spectrum 4 2.323
7
PRS047 Prostatitis 53 0.082
8
HYP056 Hypoglycemia 51 0.074
9
NRN002 Neuronitis 36 0.074
10
FCL009 Focal Dermal Hypoplasia 56 0.064
11
MLN008 Melanoma 55 0.064
12
KLP010 Klippel-Trenaunay-Weber Syndrome 54 0.064
13
P KDN018 Kidney Disease 49 0.064
14
CRB009 Cerebritis 44 0.064
15
END072 Endotheliitis 41 0.064
16
ANG062 Angioosteohypertrophic Syndrome 15 0.064
17
CLP004 Clapo Syndrome 10 0.064
18
P BRS047 Breast Cancer 100 0.052
19
P LNG032 Lung Cancer 91 0.052
20
P PRS040 Prostate Cancer 87 0.052
21
P RTN024 Retinoblastoma 73 0.052
22
P HPT021 Hepatitis 63 0.052
23
PRT036 Peritonitis 59 0.052
24
P NRF002 Neurofibromatosis 59 0.052
25
P HRT032 Heart Disease 58 0.052
26
P THY023 Thymoma 58 0.052
27
P HYD006 Hydrocephalus 58 0.052
28
TWN003 Townes-Brocks Syndrome 54 0.052
29
P BCK002 Beckwith-Wiedemann Syndrome 54 0.052
30
P GLY013 Glycogen Storage Disease 53 0.052
31
P GRV001 Graves' Disease 53 0.052
32
P PNC044 Pancreatitis 53 0.052
33
c LCL006 Localized Scleroderma 53 0.052
34
P GLM007 Glomerulonephritis 50 0.052
35
P HYP050 Hyperinsulinemic Hypoglycemia 49 0.052
36
P THY032 Thyroiditis 49 0.052
37
MLR003 Melorheostosis 47 0.052
38
OST011 Osteomalacia 44 0.052
39
P CRV039 Cervicitis 41 0.052
40
P PRK003 Parkes Weber Syndrome 36 0.052
41
MGL023 Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome, Somatic 34 0.052
42
LMB014 Limb-Body Wall Complex 28 0.052
43
MLT104 Multiple Benign Circumferential Skin Creases on Limbs 23 0.052
44
HMF005 Hemifacial Hypertrophy 17 0.052
45
SGM010 Segmental Outgrowth-Lipomatosis-Arteriovenous Malformation-Epidermal Nevus Syndrome 14 0.052
46
DYS177 Dysmorphism-Short Stature-Deafness-Disorder of Sex Development Syndrome 13 0.052
47
SPL052 Splenogonadal Fusion-Limb Defects-Micrognathia Syndrome 13 0.052
48
CLF038 Cleft Lip/palate-Deafness-Sacral Lipoma Syndrome 11 0.052
49
HPT023 Hepatocellular Carcinoma 87 0.037
50
CYS001 Cystic Fibrosis 84 0.037
51
P PNC035 Pancreatic Cancer 82 0.037
52
P OST002 Osteoporosis 76 0.037
53
HDG012 Hodgkin Lymphoma 73 0.037
54
ADR007 Adrenoleukodystrophy 71 0.037
55
ULC004 Ulcerative Colitis 70 0.037
56
P PFF001 Pfeiffer Syndrome 69 0.037
57
P MDL005 Medulloblastoma 68 0.037
58
P FML011 Familial Adenomatous Polyposis 67 0.037
59
INS024 Insulin-Like Growth Factor I 67 0.037
60
c FNC027 Fanconi Anemia, Complementation Group a 66 0.037
61
TBR010 Tuberculosis 65 0.037
62
ATT013 Attention Deficit-Hyperactivity Disorder 65 0.037
63
P WSK001 Wiskott-Aldrich Syndrome 65 0.037
64
c CNG401 Congenital Heart Disease 64 0.037
65
CNG034 Congestive Heart Failure 64 0.037
66
KWS002 Kawasaki Disease 63 0.037
67
APR006 Apert Syndrome 63 0.037
68
P LKM002 Leukemia 63 0.037
69
ANR002 Aniridia 62 0.037
70
P END044 Endometriosis 62 0.037
71
c NRF018 Neurofibromatosis, Type 1 59 0.037
72
P KDN017 Kidney Cancer 59 0.037
73
P ATS007 Autism Spectrum Disorder 59 0.037
74
P ADN016 Adenocarcinoma 59 0.037
75
P CMR001 Camurati-Engelmann Disease 58 0.037
76
P MYS003 Myasthenia Gravis 58 0.037
77
P PLY011 Polycystic Ovary Syndrome 58 0.037
78
WLM007 Wilms Tumor Susceptibility-5 58 0.037
79
LPT001 Leptospirosis 58 0.037
80
P LYM118 Lymphoma 57 0.037
81
P HMN010 Hemangioma 57 0.037
82
ART005 Arteriovenous Malformation 57 0.037
83
SCH014 Schistosomiasis 57 0.037
84
P GLB002 Glioblastoma 56 0.037
85
P GCH001 Gaucher's Disease 56 0.037
86
ATH003 Atherosclerosis 56 0.037
87
OVR029 Ovarian Hyperstimulation Syndrome 55 0.037
88
P PRM002 Primary Hyperoxaluria 55 0.037
89
PGT001 Paget's Disease of Bone 55 0.037
90
HRP004 Herpes Zoster 55 0.037
91
P HYP069 Hyperparathyroidism 54 0.037
92
P THR015 Thrombophilia 54 0.037
93
c ESS001 Essential Tremor 54 0.037
94
P HYP035 Hypophosphatasia 54 0.037
95
P INF032 Infertility 54 0.037
96
PSD014 Pseudopseudohypoparathyroidism 53 0.037
97
P PLY014 Polycystic Kidney Disease 53 0.037
98
KBG001 Kbg Syndrome 53 0.037
99
P UVT001 Uveitis 53 0.037
100
P HST010 Histiocytosis 53 0.037
101
LMY002 Leiomyoma 53 0.037
102
VSC011 Vasculitis 53 0.037
103
CFF003 Caffey Disease 52 0.037
104
P NTR004 Neutropenia 52 0.037
105
PTY003 Pityriasis Rubra Pilaris 52 0.037
106
MLG056 Malignant Hyperthermia 52 0.037
107
PPL022 Papilloma 52 0.037
108
P ESC003 Escobar Syndrome 51 0.037
109
HMF006 Hemifacial Microsomia 51 0.037
110
P LPS002 Liposarcoma 51 0.037
111
P CTS001 Cutis Laxa 51 0.037
112
LYS001 Loeys-Dietz Syndrome 51 0.037
113
DMN002 Dementia 51 0.037
114
MTH009 Mouth Disease 51 0.037
115
LYM021 Lymphadenitis 51 0.037
116
PRL032 Perlman Syndrome 50 0.037
117
P HYP004 Hypercalcemia 49 0.037
118
P HYP076 Hyperthyroidism 49 0.037
119
INS001 Insulinoma 49 0.037
120
CLT003 Colitis 49 0.037
121
IDP002 Idiopathic Juvenile Osteoporosis 49 0.037
122
P PRT013 Portal Hypertension 49 0.037
123
OST015 Osteochondrodysplasia 48 0.037
124
c PRC016 Pre-Eclampsia 48 0.037
125
MYX005 Myxoid Liposarcoma 48 0.037
126
MFF001 Maffucci Syndrome 48 0.037
127
INT079 Intrahepatic Cholangiocarcinoma 48 0.037
128
CRN248 Craniofrontonasal Dysplasia 48 0.037
129
P GST049 Gastrointestinal System Cancer 48 0.037
130
P PNM006 Pneumoconiosis 48 0.037
131
ANG020 Angiosarcoma 48 0.037
132
c PRM005 Primary Hyperparathyroidism 48 0.037
133
VGN023 Vaginitis 47 0.037
134
MLN007 Male Infertility 47 0.037
135
PRT014 Protein S Deficiency 47 0.037
136
VNB005 Van Buchem Disease 47 0.037
137
CYT008 Cytomegalovirus Infection 47 0.037
138
P ECL001 Eclampsia 47 0.037
139
PLM070 Pulmonic Stenosis 47 0.037
140
BRN004 Brain Edema 47 0.037
141
JCB001 Jacobsen Syndrome 47 0.037
142
P END033 Endocarditis 46 0.037
143
P STR022 Stargardt Disease 46 0.037
144
PLY013 Polymyalgia Rheumatica 46 0.037
145
MYL020 Myelomeningocele 45 0.037
146
SPR010 Sporotrichosis 45 0.037
147
CHL071 Child Syndrome 45 0.037
148
HDC001 Headache 45 0.037
149
PYD001 Pyoderma Gangrenosum 45 0.037
150
P AGN002 Agnosia 45 0.037
151
DYS014 Dyspepsia 45 0.037
152
OCL009 Ocular Cancer 45 0.037
153
SLR001 Sialuria 45 0.037
154
KDS001 Kid Syndrome 44 0.037
155
P MLT072 Multiple Synostoses Syndrome 44 0.037
156
GST053 Gastric Cancer 44 0.037
157
P TRM003 Tremor 44 0.037
158
HND002 Hand, Foot and Mouth Disease 44 0.037
159
HYP068 Hyperostosis 44 0.037
160
VCC001 Vaccinia 43 0.037
161
P MLT074 Multiple Endocrine Neoplasia 43 0.037
162
P MGR003 Migraine with Aura 43 0.037
163
FCL012 Facial Paralysis 43 0.037
164
GNG004 Ganglioglioma 43 0.037
165
CHR222 Chromosome 1p36 Deletion Syndrome 43 0.037
166
DVR002 Diverticulitis 43 0.037
167
P OPH004 Ophthalmoplegia 42 0.037
168
PNM001 Pneumocystosis 42 0.037
169
P STR020 Strabismus 42 0.037
170
P SCK005 Sickle Cell Disease 42 0.037
171
HLL004 Hellp Syndrome 42 0.037
172
P KLF001 Kleefstra Syndrome 41 0.037
173
MLT016 Multicentric Reticulohistiocytosis 41 0.037
174
ESN011 Eisenmenger Syndrome 41 0.037
175
INF034 Infective Endocarditis 41 0.037
176
NRL005 Neurilemmoma 41 0.037
177
IGG001 Iga Glomerulonephritis 41 0.037
178
LNR008 Linear Nevus Sebaceus Syndrome 41 0.037
179
MLN014 Melnick-Needles Syndrome 40 0.037
180
MMM001 Mammary Paget's Disease 40 0.037
181
QDR001 Quadriplegia 40 0.037
182
P PSD015 Pseudohypoparathyroidism 40 0.037
183
HPT014 Hepatorenal Syndrome 40 0.037
184
PYD002 Pyoderma 40 0.037
185
RCR004 Recurrent Respiratory Papillomatosis 40 0.037
186
FCT005 Factor Xiii Deficiency 40 0.037
187
LRN003 Learning Disability 39 0.037
188
MXD023 Mixed Cell Type Cancer 39 0.037
189
CHR008 Choroiditis 39 0.037
190
CSY001 C Syndrome 39 0.037
191
c BRC082 Brachydactyly, Type E 38 0.037
192
BCK006 Back Pain 38 0.037
193
EYD002 Eye Disease 38 0.037
194
VND001 Vein Disease 38 0.037
195
TRP014 Triploidy 38 0.037
196
BRN106 Burns 38 0.037
197
SPL006 Splenic Infarction 38 0.037
198
CLV009 Clove Syndrome, Somatic 37 0.037
199
HDN002 Head Injury 37 0.037
200
WRN004 Wrinkly Skin Syndrome 37 0.037
201
P CHN059 Chondrocalcinosis 37 0.037
202
CHR346 Chromosome 22q11.2 Deletion Syndrome, Distal 37 0.037
203
P BRN042 Branchiootic Syndrome 37 0.037
204
LYM010 Lymph Node Tuberculosis 37 0.037
205
DWR001 Dwarfism 36 0.037
206
INT042 Internuclear Ophthalmoplegia 36 0.037
207
GLC086 Glucocorticoid-Induced Osteoporosis 36 0.037
208
TRT001 Teratocarcinoma 36 0.037
209
P SPR013 Spiradenoma 35 0.037
210
P CMP008 Compartment Syndrome 35 0.037
211
URN009 Urinary System Disease 35 0.037
212
c HRD009 Hereditary Wilms' Tumor 35 0.037
213
c ART120 Arthrogryposis, Distal, Type 3 35 0.037
214
BLP005 Blepharitis 35 0.037
215
P CHN006 Chondromalacia Patellae 35 0.037
216
P LTT001 Lattice Corneal Dystrophy 34 0.037
217
P OTF002 Otofaciocervical Syndrome 34 0.037
218
HYP021 Hypercementosis 33 0.037
219
ONC003 Oncogenic Osteomalacia 33 0.037
220
BNR001 Bone Remodeling Disease 33 0.037
221
HMF004 Hemifacial Spasm 32 0.037
222
ZYG002 Zygomycosis 32 0.037
223
c PST005 Posterior Uveitis 32 0.037
224
BNR002 Bone Resorption Disease 32 0.037
225
MNM001 Monomelic Amyotrophy 32 0.037
226
MDS022 Mediastinitis 32 0.037
227
CHR356 Chromosome 3q29 Microdeletion Syndrome 32 0.037
228
PRG031 Progressive Hemifacial Atrophy 31 0.037
229
PRS051 Parastremmatic Dwarfism 31 0.037
230
AXL003 Axial Osteomalacia 31 0.037
231
ISC005 Ischemic Bone Disease 31 0.037
232
CRR004 Currarino Triad 30 0.037
233
MLN013 Melanoma Metastasis 30 0.037
234
CHN011 Chondromalacia 30 0.037
235
VLV008 Vulvitis 30 0.037
236
CHR391 Chromosome 15q24 Deletion Syndrome 30 0.037
237
MLK004 Malakoplakia 30 0.037
238
ATN005 Autonomic Dysfunction 30 0.037
239
HRP002 Herpes Gestationis 30 0.037
240
GLS018 Glass Syndrome 29 0.037
241
LTR002 Lateral Sinus Thrombosis 29 0.037
242
FCL011 Facial Nerve Disease 29 0.037
243
CPL011 Capillary Malformations, Congenital, 1, Somatic, Mosaic 29 0.037
244
48X003 48,xxyy Syndrome 28 0.037
245
VSL003 Visual Agnosia 28 0.037
246
PHC006 Phacomatosis Pigmentovascularis 28 0.037
247
WRT001 Worth's Syndrome 28 0.037
248
TTR014 Tetrasomy 18p 28 0.037
249
TMT003 Temtamy Syndrome 27 0.037
250
IMP003 Impaired Renal Function Disease 27 0.037
251
c SPN104 Spinocerebellar Ataxia 34 27 0.037
252
MRC001 Marchiafava Bignami Disease 26 0.037
253
GNS002 Genoa Syndrome 26 0.037
254
P PRT063 Proteus-Like Syndrome 25 0.037
255
WLD004 Wildervanck Syndrome 25 0.037
256
PLM007 Pulmonary Aspergilloma 25 0.037
257
MSC016 Mosaic Trisomy 14 25 0.037
258
c ORF033 Orofaciodigital Syndrome V 24 0.037
259
IRS003 Iris Disease 23 0.037
260
ISL096 Isolated Klippel-Feil Syndrome 23 0.037
261
c ANT010 Anterior Compartment Syndrome 23 0.037
262
AXL004 Axial Mesodermal Dysplasia Spectrum 23 0.037
263
GRN016 Grant Syndrome 23 0.037
264
c CHN018 Chondrodysplasia Punctata 2, X-Linked 23 0.037
265
RGN005 Regional Odontodysplasia 23 0.037
266
HYP654 Hypoglossia-Hypodactyly Syndrome 23 0.037
267
FNL001 Fine-Lubinsky Syndrome 22 0.037
268
FRN022 Frontofacionasal Dysplasia 22 0.037
269
TLH001 Tel Hashomer Camptodactyly Syndrome 22 0.037
270
PGD001 Pagod Syndrome 21 0.037
271
GLB003 Globe Disease 21 0.037
272
CRR005 Curry Jones Syndrome 20 0.037
273
ISL062 Isolated Plagiocephaly 20 0.037
274
MCR089 Microsomia Hemifacial Radial Defects 20 0.037
275
ART046 Arthrogryposis Multiplex Congenita Neurogenic Type 19 0.037
276
RMB001 Rombo Syndrome 19 0.037
277
CRN083 Craniofacial Dyssynostosis 19 0.037
278
HMR016 Humeroradioulnar Synostosis 18 0.037
279
2Q3005 2q31.1 Microdeletion Syndrome 18 0.037
280
TBT001 Tabatznik Syndrome 18 0.037
281
CNT067 Central Cord Syndrome 18 0.037
282
DYS134 Dysspondyloenchondromatosis 17 0.037
283
P FML153 Familial Wilms Tumor 17 0.037
284
JRG001 Jorgenson Lenz Syndrome 17 0.037
285
P NNT037 Neonatal Inflammatory Skin and Bowel Disease 17 0.037
286
TRT006 Torticollis Keloids Cryptorchidism Renal Dysplasia 16 0.037
287
JHN004 Johnson Neuroectodermal Syndrome 16 0.037
288
CHR416 Chromosome 17q Deletion 15 0.037
289
XLN073 X-Linked Mandibulofacial Dysostosis 15 0.037
290
DST036 Distal Trisomy 15q 15 0.037
291
48X002 48,xxxy Syndrome 15 0.037
292
HYP664 Hypertrichosis Cubiti-Short Stature Syndrome 15 0.037
293
SPN145 Spondylometaphyseal Dysplasia Corner Fracture Type 15 0.037
294
MST010 Mastocytosis Cutaneous with Short Stature Conductive Hearing Loss and Microtia 15 0.037
295
DFN300 Deafness-Genital Anomalies-Metacarpal and Metatarsal Synostosis Syndrome 14 0.037
296
RZN001 Rozin Hertz Goodman Syndrome 14 0.037
297
EPP005 Epiphyseal Dysplasia Hearing Loss Dysmorphism 14 0.037
298
PLT011 Pilotto Syndrome 14 0.037
299
INT231 Intellectual Disability - Athetosis - Microphthalmia 14 0.037
300
CLF019 Cleft Palate Short Stature Vertebral Anomalies 13 0.037
301
MLG089 Malignant Hyperthermia Arthrogryposis Torticollis 13 0.037
302
ART113 Aortic Arch Anomaly - Peculiar Facies - Intellectual Disability 13 0.037
303
THR030 Thoraco Abdominal Enteric Duplication 13 0.037
304
DFN006 Deafness Craniofacial Syndrome 12 0.037
305
CNG240 Congenital Unilateral Hypoplasia of Depressor Anguli Oris 12 0.037
306
OSL002 O'sullivan-Mcleod Syndrome 12 0.037
307
FRS008 Froster-Huch Syndrome 12 0.037
308
TRP011 Triopia 11 0.037
309
MCR293 Microcephaly-Deafness-Intellectual Disability Syndrome 11 0.037
310
INT287 Intellectual Disability-Hypotonia-Skin Hyperpigmentation Syndrome 11 0.037
311
DLY007 Delayed Speech-Facial Asymmetry-Strabismus-Ear Lobe Creases Syndrome 11 0.037
312
LWR015 Lower Limb Deficiency-Hypospadias Syndrome 11 0.037
313
HMF002 Hemifacial Hyperplasia Strabismus 11 0.037
314
HM3001 Hemi 3 Syndrome 10 0.037
315
c FML203 Familial Lambdoid Synostosis 10 0.037
316
INT291 Intellectual Disability-Myopathy-Short Stature-Endocrine Defect Syndrome 10 0.037
317
VLF002 Velo-Facial-Skeletal Syndrome 10 0.037
318
MXD009 Mixed Cell Type Kidney Wilms' Tumor 10 0.037
319
XLN131 X-Linked Intellectual Disability, Miles-Carpenter Type 8 0.037
320
ANG035 Angiokeratoma Corporis Diffusum with Arteriovenous Fistulas 8 0.037
321
UVL003 Uveal Diseases 4 0.037