Search results for "hemihypertrophy"

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

116 hits were found for 'hemihypertrophy'

# Family MCID Name MIFTS Score
1
HMH002 Hemihypertrophy 39 6.237
2
HYP524 Hypoinsulinemic Hypoglycemia with Hemihypertrophy 14 5.993
3
PRT093 Proteus Syndrome, Somatic 55 4.866
4
HMH004 Hemihyperplasia, Isolated 23 2.561
5
MCR030 Macrocephaly Mesodermal Hamartoma Spectrum 3 2.410
6
P BCK002 Beckwith-Wiedemann Syndrome 56 0.188
7
MDL009 Medullary Sponge Kidney 40 0.188
8
HMM003 Hemimegalencephaly 45 0.173
9
ANR002 Aniridia 60 0.128
10
P PHC003 Pheochromocytoma 71 0.117
11
ADN018 Adenoma 59 0.117
12
P SCL018 Scoliosis 56 0.117
13
HPT022 Hepatoblastoma 53 0.117
14
CRB009 Cerebritis 38 0.117
15
RHB003 Rhabdomyosarcoma 58 0.104
16
KLP010 Klippel-Trenaunay-Weber Syndrome 54 0.104
17
LPM005 Lipomatosis 47 0.104
18
VSC047 Vascular Malformation 45 0.104
19
WBR001 Weber Syndrome 37 0.104
20
P RNL014 Renal Cell Carcinoma 81 0.090
21
P HRT032 Heart Disease 76 0.090
22
P ADN016 Adenocarcinoma 69 0.090
23
P HYP060 Hyperinsulinism 59 0.090
24
CLR003 Clear Cell Adenocarcinoma 54 0.090
25
HYP077 Hypertrichosis 52 0.090
26
HMF009 Hemifacial Hyperplasia 32 0.090
27
ANG062 Angioosteohypertrophic Syndrome 14 0.090
28
CPL012 Capillary Malformation of the Lower Lip, Lymphatic Malformation of Face and Neck, Asymmetry of Face and Limbs, and Partial/generalized Overgrowth 11 0.090
29
P BRS047 Breast Cancer 100 0.074
30
P HPT021 Hepatitis 70 0.074
31
P LKM002 Leukemia 70 0.074
32
P HYD006 Hydrocephalus 67 0.074
33
P EPL164 Epilepsy 66 0.074
34
SRC014 Sarcoma 66 0.074
35
ACR007 Acromegaly 65 0.074
36
ART005 Arteriovenous Malformation 65 0.074
37
WLM007 Wilms Tumor Susceptibility-5 64 0.074
38
ACN011 Acne 63 0.074
39
P LYM025 Lymphedema 61 0.074
40
P HMN010 Hemangioma 60 0.074
41
INC021 Incontinentia Pigmenti 60 0.074
42
P RCK004 Rickets 59 0.074
43
ACN002 Acanthosis Nigricans 57 0.074
44
ADR005 Adrenal Carcinoma 56 0.074
45
P PLY006 Polydactyly 55 0.074
46
LYM022 Lymphangioma 54 0.074
47
P EMB005 Embryonal Rhabdomyosarcoma 54 0.074
48
c CNT075 Central Precocious Puberty 53 0.074
49
P HLL001 Hallermann-Streiff Syndrome 53 0.074
50
NTH001 Netherton Syndrome 52 0.074
51
P PRC019 Precocious Puberty 51 0.074
52
P HYP613 Hypophosphatemic Rickets 51 0.074
53
P OVR046 Ovarian Cyst 50 0.074
54
FLL008 Folliculitis 47 0.074
55
ADR008 Adrenal Adenoma 46 0.074
56
HMN009 Hemangioblastoma 45 0.074
57
RNL078 Renal Dysplasia 45 0.074
58
CLV009 Clove Syndrome, Somatic 42 0.074
59
PRT019 Protein-Losing Enteropathy 41 0.074
60
c HRD009 Hereditary Wilms' Tumor 41 0.074
61
IDP070 Idiopathic Scoliosis 40 0.074
62
RTR010 Retroperitoneal Sarcoma 39 0.074
63
c CNG029 Congenital Mesoblastic Nephroma 39 0.074
64
HMN016 Hemangioendothelioma 38 0.074
65
EMB002 Embryoma 34 0.074
66
P MSN006 Mesenchymoma 32 0.074
67
THY043 Thymic Hyperplasia 32 0.074
68
CYS019 Cystathioninuria 29 0.074
69
GGN002 Gigantism 27 0.074
70
MTN001 Metanephric Adenoma 27 0.074
71
c BNG012 Benign Mesenchymoma 26 0.074
72
P PRT063 Proteus-Like Syndrome 14 0.074
73
CHL076 Chilaiditi Syndrome 14 0.074
74
MSC081 Mosaic Trisomy 15 13 0.074
75
PHC005 Phacomatosis Pigmentokeratotica 12 0.074
76
HM3001 Hemi 3 Syndrome 7 0.074
77
P KDN017 Kidney Cancer 67 0.052
78
P CSH001 Cushing's Syndrome 64 0.052
79
EYD002 Eye Disease 63 0.052
80
OCL009 Ocular Cancer 62 0.052
81
HYP056 Hypoglycemia 61 0.052
82
ETH011 Ethylmalonic Encephalopathy 59 0.052
83
ABL002 Ablepharon-Macrostomia Syndrome 57 0.052
84
PRL032 Perlman Syndrome 55 0.052
85
P RNL100 Renal Hypodysplasia/aplasia 1 54 0.052
86
ADR044 Adrenal Insufficiency, Congenital, with 46xy Sex Reversal, Partial or Complete 53 0.052
87
URN009 Urinary System Disease 53 0.052
88
WHM001 Whim Syndrome 52 0.052
89
VND001 Vein Disease 52 0.052
90
EPD053 Epidermal Nevus, Somatic 51 0.052
91
LRN003 Learning Disability 51 0.052
92
CSY001 C Syndrome 49 0.052
93
HND003 Hand-Foot-Uterus Syndrome 47 0.052
94
BRL010 Buruli Ulcer 47 0.052
95
MXD023 Mixed Cell Type Cancer 47 0.052
96
ACR041 Acromelic Frontonasal Dysostosis 46 0.052
97
BRC085 Brca2 Hereditary Breast and Ovarian Cancer Syndrome 44 0.052
98
CRP017 Carpal Tunnel Syndrome, Familial 44 0.052
99
BRT030 Birth Defects 43 0.052
100
GLB003 Globe Disease 35 0.052
101
IRS003 Iris Disease 32 0.052
102
MGL023 Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome, Somatic 32 0.052
103
CVT001 Cavitary Optic Disc Anomalies 32 0.052
104
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 31 0.052
105
CYL001 Cayler Cardiofacial Syndrome 30 0.052
106
MNN028 Mononeuropathy of the Median Nerve, Mild 29 0.052
107
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 29 0.052
108
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 26 0.052
109
P LYM124 Lymphangiectasia, Intestinal 25 0.052
110
RHB020 Rhabdomyosarcoma, Somatic 23 0.052
111
HYP213 Hypomelanotic Disorder 21 0.052
112
P FML153 Familial Wilms Tumor 20 0.052
113
MXD009 Mixed Cell Type Kidney Wilms' Tumor 17 0.052
114
VSC050 Vascular Malformation, Primary Intraosseous 15 0.052
115
UVL003 Uveal Diseases 14 0.052
116
ANG035 Angiokeratoma Corporis Diffusum with Arteriovenous Fistulas 7 0.052