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 37 6.130
2
HYP524 Hypoinsulinemic Hypoglycemia with Hemihypertrophy 15 5.336
3
PRT093 Proteus Syndrome, Somatic 54 4.754
4
HMH004 Hemihyperplasia, Isolated 23 2.515
5
HMH001 Hemihypertrophy Intestinal Web Corneal Opacity 3 2.420
6
MCR030 Macrocephaly Mesodermal Hamartoma Spectrum 4 2.343
7
P BCK002 Beckwith-Wiedemann Syndrome 56 0.196
8
MDL009 Medullary Sponge Kidney 41 0.196
9
HMM003 Hemimegalencephaly 47 0.182
10
ANR002 Aniridia 62 0.139
11
P PHC003 Pheochromocytoma 72 0.128
12
P SCL018 Scoliosis 56 0.128
13
HPT022 Hepatoblastoma 57 0.128
14
ADN018 Adenoma 59 0.128
15
CRB009 Cerebritis 36 0.128
16
KLP010 Klippel-Trenaunay-Weber Syndrome 53 0.117
17
RHB003 Rhabdomyosarcoma 55 0.117
18
LPM005 Lipomatosis 46 0.117
19
WBR001 Weber Syndrome 36 0.117
20
VSC047 Vascular Malformation 45 0.117
21
P RNL014 Renal Cell Carcinoma 80 0.105
22
c CNG401 Congenital Heart Disease 67 0.105
23
HYP077 Hypertrichosis 52 0.105
24
HMF009 Hemifacial Hyperplasia 31 0.105
25
P ADN016 Adenocarcinoma 69 0.105
26
P HRT032 Heart Disease 64 0.105
27
P HYP060 Hyperinsulinism 58 0.105
28
CLR003 Clear Cell Adenocarcinoma 52 0.105
29
P BRS047 Breast Cancer 100 0.091
30
WLM007 Wilms Tumor Susceptibility-5 64 0.091
31
ACN011 Acne 63 0.091
32
INC021 Incontinentia Pigmenti 57 0.091
33
P HYD006 Hydrocephalus 68 0.091
34
P NRF002 Neurofibromatosis 66 0.091
35
ACR007 Acromegaly 66 0.091
36
NTH001 Netherton Syndrome 52 0.091
37
P RCK004 Rickets 59 0.091
38
P PRC019 Precocious Puberty 53 0.091
39
P HPT021 Hepatitis 74 0.091
40
P LKM002 Leukemia 70 0.091
41
ART005 Arteriovenous Malformation 63 0.091
42
P HLL001 Hallermann-Streiff Syndrome 53 0.091
43
P PLY006 Polydactyly 56 0.091
44
P HYP613 Hypophosphatemic Rickets 50 0.091
45
ADR005 Adrenal Carcinoma 57 0.091
46
SRC014 Sarcoma 66 0.091
47
ACN002 Acanthosis Nigricans 59 0.091
48
P HMN010 Hemangioma 62 0.091
49
CYS019 Cystathioninuria 30 0.091
50
P LYM025 Lymphedema 60 0.091
51
P EMB005 Embryonal Rhabdomyosarcoma 56 0.091
52
LYM022 Lymphangioma 55 0.091
53
P OVR046 Ovarian Cyst 48 0.091
54
ADR008 Adrenal Adenoma 49 0.091
55
RNL078 Renal Dysplasia 48 0.091
56
P PRT063 Proteus-Like Syndrome 17 0.091
57
c CNT075 Central Precocious Puberty 49 0.091
58
P EPL164 Epilepsy 60 0.091
59
HMN009 Hemangioblastoma 45 0.091
60
EMB002 Embryoma 33 0.091
61
PRT019 Protein-Losing Enteropathy 42 0.091
62
c CNG029 Congenital Mesoblastic Nephroma 37 0.091
63
FLL008 Folliculitis 47 0.091
64
CPL012 Capillary Malformation of the Lower Lip, Lymphatic Malformation of Face and Neck, Asymmetry of Face and Limbs, and Partial/generalized Overgrowth 11 0.091
65
MTN001 Metanephric Adenoma 28 0.091
66
RTR010 Retroperitoneal Sarcoma 39 0.091
67
GGN002 Gigantism 29 0.091
68
THY043 Thymic Hyperplasia 32 0.091
69
c BNG012 Benign Mesenchymoma 25 0.091
70
ANG062 Angioosteohypertrophic Syndrome 14 0.091
71
CHL076 Chilaiditi Syndrome 14 0.091
72
HM3001 Hemi 3 Syndrome 5 0.091
73
HMN016 Hemangioendothelioma 40 0.091
74
PHC005 Phacomatosis Pigmentokeratotica 12 0.091
75
IDP070 Idiopathic Scoliosis 38 0.091
76
MSC081 Mosaic Trisomy 15 14 0.091
77
P MSN006 Mesenchymoma 31 0.091
78
P CSH001 Cushing's Syndrome 65 0.074
79
P RNL100 Renal Hypodysplasia/aplasia 1 54 0.074
80
CLV009 Clove Syndrome, Somatic 41 0.074
81
WHM001 Whim Syndrome 53 0.074
82
ADR044 Adrenal Insufficiency, Congenital, with 46xy Sex Reversal, Partial or Complete 36 0.074
83
BRL010 Buruli Ulcer 47 0.074
84
HYP056 Hypoglycemia 60 0.074
85
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 26 0.074
86
MNN028 Mononeuropathy of the Median Nerve, Mild 26 0.074
87
c CTS029 Cutis Laxa, Autosomal Recessive, Type Iiia 34 0.074
88
RHB020 Rhabdomyosarcoma, Somatic 23 0.074
89
CYL001 Cayler Cardiofacial Syndrome 30 0.074
90
VSC050 Vascular Malformation, Primary Intraosseous 13 0.074
91
HYP213 Hypomelanotic Disorder 20 0.074
92
P KDN017 Kidney Cancer 67 0.052
93
ETH011 Ethylmalonic Encephalopathy 57 0.052
94
P URF003 Urofacial Syndrome 1 51 0.052
95
MGL023 Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome, Somatic 34 0.052
96
CSY001 C Syndrome 49 0.052
97
PRL032 Perlman Syndrome 55 0.052
98
ACR041 Acromelic Frontonasal Dysostosis 45 0.052
99
HND003 Hand-Foot-Uterus Syndrome 46 0.052
100
URN009 Urinary System Disease 52 0.052
101
ABL002 Ablepharon-Macrostomia Syndrome 51 0.052
102
EYD002 Eye Disease 62 0.052
103
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 35 0.052
104
OCL009 Ocular Cancer 61 0.052
105
LRN003 Learning Disability 49 0.052
106
VND001 Vein Disease 51 0.052
107
CVT001 Cavitary Optic Disc Anomalies 25 0.052
108
BRT030 Birth Defects 44 0.052
109
MXD023 Mixed Cell Type Cancer 45 0.052
110
c HRD009 Hereditary Wilms' Tumor 40 0.052
111
GLB003 Globe Disease 34 0.052
112
MXD009 Mixed Cell Type Kidney Wilms' Tumor 16 0.052
113
IRS003 Iris Disease 32 0.052
114
ANG035 Angiokeratoma Corporis Diffusum with Arteriovenous Fistulas 8 0.052
115
P FML153 Familial Wilms Tumor 19 0.052
116
UVL003 Uveal Diseases 12 0.052