Search results for "hemihypertrophy"

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

232 hits were found for 'hemihypertrophy'

# Family MCID Name MIFTS Score
1
HYP524 Hypoinsulinemic Hypoglycemia with Hemihypertrophy 14 5.292
2
PRT093 Proteus Syndrome, Somatic 55 4.718
3
ISL101 Isolated Hemihyperplasia 27 2.415
4
HYP493 Hypoinsulinemic Hypoglycemia and Body Hemihypertrophy 4 2.393
5
HMH001 Hemihypertrophy Intestinal Web Corneal Opacity 3 2.393
6
MCR030 Macrocephaly Mesodermal Hamartoma Spectrum 4 2.332
7
MDL009 Medullary Sponge Kidney 42 0.138
8
P BCK002 Beckwith-Wiedemann Syndrome 54 0.132
9
HMM003 Hemimegalencephaly 44 0.132
10
ANR002 Aniridia 60 0.093
11
KLP010 Klippel-Trenaunay-Weber Syndrome 56 0.093
12
P PHC003 Pheochromocytoma 71 0.083
13
ADN018 Adenoma 62 0.083
14
HPT022 Hepatoblastoma 55 0.083
15
P SCL018 Scoliosis 51 0.083
16
CRB009 Cerebritis 48 0.083
17
RHB003 Rhabdomyosarcoma 58 0.072
18
FCL009 Focal Dermal Hypoplasia 54 0.072
19
LPM005 Lipomatosis 47 0.072
20
WBR001 Weber Syndrome 40 0.072
21
VSC047 Vascular Malformation 38 0.072
22
ANG062 Angioosteohypertrophic Syndrome 16 0.072
23
CLP004 Clapo Syndrome 10 0.072
24
P RNL014 Renal Cell Carcinoma 80 0.059
25
c CNG401 Congenital Heart Disease 70 0.059
26
P ADN016 Adenocarcinoma 69 0.059
27
P HRT032 Heart Disease 68 0.059
28
c LCL006 Localized Scleroderma 61 0.059
29
HYP056 Hypoglycemia 60 0.059
30
P HYP060 Hyperinsulinism 58 0.059
31
CLR003 Clear Cell Adenocarcinoma 57 0.059
32
TWN003 Townes-Brocks Syndrome 54 0.059
33
HYP077 Hypertrichosis 43 0.059
34
MLR003 Melorheostosis 43 0.059
35
P INT191 Intestinal Lymphangiectasia 39 0.059
36
P PRK003 Parkes Weber Syndrome 37 0.059
37
MGL023 Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome, Somatic 32 0.059
38
LMB014 Limb-Body Wall Complex 28 0.059
39
P PRT063 Proteus-Like Syndrome 25 0.059
40
MLT104 Multiple Benign Circumferential Skin Creases on Limbs 24 0.059
41
SGM010 Segmental Outgrowth-Lipomatosis-Arteriovenous Malformation-Epidermal Nevus Syndrome 16 0.059
42
HMF005 Hemifacial Hypertrophy 16 0.059
43
DYS177 Dysmorphism-Short Stature-Deafness-Disorder of Sex Development Syndrome 14 0.059
44
SPL052 Splenogonadal Fusion-Limb Defects-Micrognathia Syndrome 13 0.059
45
HM3001 Hemi 3 Syndrome 13 0.059
46
CLF038 Cleft Lip/palate-Deafness-Sacral Lipoma Syndrome 11 0.059
47
P BRS047 Breast Cancer 100 0.042
48
P OST002 Osteoporosis 80 0.042
49
P HPT021 Hepatitis 77 0.042
50
P NRF002 Neurofibromatosis 74 0.042
51
P PFF001 Pfeiffer Syndrome 72 0.042
52
c FNC027 Fanconi Anemia, Complementation Group a 71 0.042
53
P LKM002 Leukemia 70 0.042
54
P PRM002 Primary Hyperoxaluria 70 0.042
55
ART005 Arteriovenous Malformation 68 0.042
56
P KDN017 Kidney Cancer 67 0.042
57
APR006 Apert Syndrome 67 0.042
58
P HYD006 Hydrocephalus 66 0.042
59
ACR007 Acromegaly 66 0.042
60
P CMR001 Camurati-Engelmann Disease 66 0.042
61
EYD002 Eye Disease 65 0.042
62
SRC014 Sarcoma 65 0.042
63
ACN011 Acne 65 0.042
64
PGT001 Paget's Disease of Bone 64 0.042
65
OCL009 Ocular Cancer 63 0.042
66
WLM007 Wilms Tumor Susceptibility-5 63 0.042
67
P GCH001 Gaucher's Disease 62 0.042
68
P RCK004 Rickets 62 0.042
69
P HMN010 Hemangioma 62 0.042
70
P GST049 Gastrointestinal System Cancer 61 0.042
71
P KDN018 Kidney Disease 60 0.042
72
P LYM025 Lymphedema 60 0.042
73
P ESC003 Escobar Syndrome 59 0.042
74
INT079 Intrahepatic Cholangiocarcinoma 59 0.042
75
ADR005 Adrenal Carcinoma 59 0.042
76
HMF006 Hemifacial Microsomia 58 0.042
77
PRL032 Perlman Syndrome 58 0.042
78
ACN002 Acanthosis Nigricans 57 0.042
79
INC021 Incontinentia Pigmenti 56 0.042
80
P EMB005 Embryonal Rhabdomyosarcoma 55 0.042
81
P HLL001 Hallermann-Streiff Syndrome 55 0.042
82
MRC001 Marchiafava Bignami Disease 54 0.042
83
P SPR013 Spiradenoma 54 0.042
84
IDP002 Idiopathic Juvenile Osteoporosis 54 0.042
85
ADR008 Adrenal Adenoma 54 0.042
86
OST015 Osteochondrodysplasia 54 0.042
87
CHL071 Child Syndrome 54 0.042
88
P PLY006 Polydactyly 54 0.042
89
FCL012 Facial Paralysis 53 0.042
90
P PRC019 Precocious Puberty 53 0.042
91
VND001 Vein Disease 53 0.042
92
KDS001 Kid Syndrome 52 0.042
93
KBG001 Kbg Syndrome 52 0.042
94
LYM022 Lymphangioma 52 0.042
95
LRN003 Learning Disability 51 0.042
96
LYS001 Loeys-Dietz Syndrome 51 0.042
97
URN009 Urinary System Disease 51 0.042
98
P HYP613 Hypophosphatemic Rickets 51 0.042
99
HMN009 Hemangioblastoma 51 0.042
100
CFF003 Caffey Disease 50 0.042
101
MXD023 Mixed Cell Type Cancer 50 0.042
102
P HYP035 Hypophosphatasia 50 0.042
103
MFF001 Maffucci Syndrome 50 0.042
104
OST011 Osteomalacia 50 0.042
105
FLL008 Folliculitis 50 0.042
106
HYP068 Hyperostosis 49 0.042
107
CSY001 C Syndrome 49 0.042
108
c CNT075 Central Precocious Puberty 48 0.042
109
NTH001 Netherton Syndrome 48 0.042
110
ESN011 Eisenmenger Syndrome 48 0.042
111
INC001 Incontinentia Pigmenti Achromians 47 0.042
112
VNB005 Van Buchem Disease 47 0.042
113
P MLT072 Multiple Synostoses Syndrome 46 0.042
114
P OVR046 Ovarian Cyst 46 0.042
115
JCB001 Jacobsen Syndrome 46 0.042
116
CRN248 Craniofrontonasal Dysplasia 45 0.042
117
c HRD009 Hereditary Wilms' Tumor 44 0.042
118
PRT019 Protein-Losing Enteropathy 44 0.042
119
LNR008 Linear Nevus Sebaceus Syndrome 44 0.042
120
RTR010 Retroperitoneal Sarcoma 43 0.042
121
P CHN059 Chondrocalcinosis 43 0.042
122
BNR001 Bone Remodeling Disease 43 0.042
123
c CNG029 Congenital Mesoblastic Nephroma 42 0.042
124
GLC086 Glucocorticoid-Induced Osteoporosis 42 0.042
125
c ART120 Arthrogryposis, Distal, Type 3 42 0.042
126
FCL011 Facial Nerve Disease 42 0.042
127
CHR222 Chromosome 1p36 Deletion Syndrome 42 0.042
128
IDP070 Idiopathic Scoliosis 42 0.042
129
BNR002 Bone Resorption Disease 42 0.042
130
RNL078 Renal Dysplasia 41 0.042
131
ISC005 Ischemic Bone Disease 40 0.042
132
P KLF001 Kleefstra Syndrome 40 0.042
133
HMN016 Hemangioendothelioma 40 0.042
134
c BRC082 Brachydactyly, Type E 38 0.042
135
IMP003 Impaired Renal Function Disease 38 0.042
136
CPL011 Capillary Malformations, Congenital, 1, Somatic, Mosaic 38 0.042
137
MLN014 Melnick-Needles Syndrome 38 0.042
138
PRG031 Progressive Hemifacial Atrophy 37 0.042
139
CHR346 Chromosome 22q11.2 Deletion Syndrome, Distal 37 0.042
140
GLS018 Glass Syndrome 37 0.042
141
HYP021 Hypercementosis 36 0.042
142
CHY006 Chylous Ascites 36 0.042
143
P LTT001 Lattice Corneal Dystrophy 35 0.042
144
WRN004 Wrinkly Skin Syndrome 35 0.042
145
EMB002 Embryoma 34 0.042
146
P BRN042 Branchiootic Syndrome 34 0.042
147
AXL003 Axial Osteomalacia 34 0.042
148
WRT001 Worth's Syndrome 34 0.042
149
IRS003 Iris Disease 33 0.042
150
P MSN006 Mesenchymoma 33 0.042
151
CYS019 Cystathioninuria 33 0.042
152
P GGN002 Gigantism 33 0.042
153
P OTF002 Otofaciocervical Syndrome 33 0.042
154
THY043 Thymic Hyperplasia 33 0.042
155
GLB003 Globe Disease 32 0.042
156
MNM001 Monomelic Amyotrophy 32 0.042
157
CHR356 Chromosome 3q29 Microdeletion Syndrome 31 0.042
158
CHR391 Chromosome 15q24 Deletion Syndrome 30 0.042
159
PRS051 Parastremmatic Dwarfism 30 0.042
160
48X003 48,xxyy Syndrome 30 0.042
161
GNS002 Genoa Syndrome 29 0.042
162
c BNG012 Benign Mesenchymoma 29 0.042
163
PHC006 Phacomatosis Pigmentovascularis 28 0.042
164
CLV009 Clove Syndrome, Somatic 27 0.042
165
TTR014 Tetrasomy 18p 27 0.042
166
GRN016 Grant Syndrome 26 0.042
167
TMT003 Temtamy Syndrome 26 0.042
168
CRR004 Currarino Triad 26 0.042
169
WLD004 Wildervanck Syndrome 26 0.042
170
c CHN018 Chondrodysplasia Punctata 2, X-Linked 26 0.042
171
c SPN104 Spinocerebellar Ataxia 34 25 0.042
172
c ORF033 Orofaciodigital Syndrome V 25 0.042
173
JHN004 Johnson Neuroectodermal Syndrome 25 0.042
174
ISL096 Isolated Klippel-Feil Syndrome 25 0.042
175
MTN001 Metanephric Adenoma 25 0.042
176
FNL001 Fine-Lubinsky Syndrome 24 0.042
177
MSC016 Mosaic Trisomy 14 24 0.042
178
P FML153 Familial Wilms Tumor 23 0.042
179
FRN022 Frontofacionasal Dysplasia 23 0.042
180
HYP654 Hypoglossia-Hypodactyly Syndrome 23 0.042
181
P NNT037 Neonatal Inflammatory Skin and Bowel Disease 22 0.042
182
TLH001 Tel Hashomer Camptodactyly Syndrome 22 0.042
183
AXL004 Axial Mesodermal Dysplasia Spectrum 21 0.042
184
PGD001 Pagod Syndrome 21 0.042
185
ISL062 Isolated Plagiocephaly 21 0.042
186
MCR089 Microsomia Hemifacial Radial Defects 21 0.042
187
CRR005 Curry Jones Syndrome 21 0.042
188
RMB001 Rombo Syndrome 20 0.042
189
CRN083 Craniofacial Dyssynostosis 20 0.042
190
ART046 Arthrogryposis Multiplex Congenita Neurogenic Type 19 0.042
191
HMR016 Humeroradioulnar Synostosis 19 0.042
192
JRG001 Jorgenson Lenz Syndrome 19 0.042
193
DYS134 Dysspondyloenchondromatosis 19 0.042
194
MXD009 Mixed Cell Type Kidney Wilms' Tumor 19 0.042
195
TBT001 Tabatznik Syndrome 18 0.042
196
2Q3005 2q31.1 Microdeletion Syndrome 18 0.042
197
TRT006 Torticollis Keloids Cryptorchidism Renal Dysplasia 18 0.042
198
CHL076 Chilaiditi Syndrome 17 0.042
199
MSC081 Mosaic Trisomy 15 17 0.042
200
XLN073 X-Linked Mandibulofacial Dysostosis 16 0.042
201
48X002 48,xxxy Syndrome 16 0.042
202
DST036 Distal Trisomy 15q 16 0.042
203
CHR416 Chromosome 17q Deletion 16 0.042
204
PHC005 Phacomatosis Pigmentokeratotica 16 0.042
205
HYP664 Hypertrichosis Cubiti-Short Stature Syndrome 16 0.042
206
SPN145 Spondylometaphyseal Dysplasia Corner Fracture Type 16 0.042
207
DFN300 Deafness-Genital Anomalies-Metacarpal and Metatarsal Synostosis Syndrome 16 0.042
208
DFN006 Deafness Craniofacial Syndrome 16 0.042
209
RZN001 Rozin Hertz Goodman Syndrome 15 0.042
210
MST010 Mastocytosis Cutaneous with Short Stature Conductive Hearing Loss and Microtia 15 0.042
211
THR030 Thoraco Abdominal Enteric Duplication 15 0.042
212
EPP005 Epiphyseal Dysplasia Hearing Loss Dysmorphism 15 0.042
213
PLT011 Pilotto Syndrome 15 0.042
214
INT231 Intellectual Disability - Athetosis - Microphthalmia 15 0.042
215
UVL003 Uveal Diseases 14 0.042
216
CLF019 Cleft Palate Short Stature Vertebral Anomalies 14 0.042
217
MLG089 Malignant Hyperthermia Arthrogryposis Torticollis 14 0.042
218
ART113 Aortic Arch Anomaly - Peculiar Facies - Intellectual Disability 14 0.042
219
CNG240 Congenital Unilateral Hypoplasia of Depressor Anguli Oris 13 0.042
220
OSL002 O'sullivan-Mcleod Syndrome 13 0.042
221
MCR293 Microcephaly-Deafness-Intellectual Disability Syndrome 12 0.042
222
FRS008 Froster-Huch Syndrome 12 0.042
223
DLY007 Delayed Speech-Facial Asymmetry-Strabismus-Ear Lobe Creases Syndrome 12 0.042
224
TRP011 Triopia 12 0.042
225
HMF002 Hemifacial Hyperplasia Strabismus 12 0.042
226
INT291 Intellectual Disability-Myopathy-Short Stature-Endocrine Defect Syndrome 12 0.042
227
INT287 Intellectual Disability-Hypotonia-Skin Hyperpigmentation Syndrome 12 0.042
228
LWR015 Lower Limb Deficiency-Hypospadias Syndrome 11 0.042
229
c FML203 Familial Lambdoid Synostosis 11 0.042
230
VLF002 Velo-Facial-Skeletal Syndrome 11 0.042
231
XLN131 X-Linked Intellectual Disability, Miles-Carpenter Type 9 0.042
232
ANG035 Angiokeratoma Corporis Diffusum with Arteriovenous Fistulas 7 0.042