Search results for hemihypertrophy

122 hits were found for hemihypertrophy

# Family MCID Name MIFTS Score
1
HMH002 Hemihypertrophy 41 6.238
2
HYP524 Hypoinsulinemic Hypoglycemia with Hemihypertrophy 16 6.015
3
PRT093 Proteus Syndrome, Somatic 56 4.872
4
HMH004 Hemihyperplasia, Isolated 23 2.582
5
MCR030 Macrocephaly Mesodermal Hamartoma Spectrum 3 2.413
6
P BCK002 Beckwith-Wiedemann Syndrome 56 0.193
7
MDL009 Medullary Sponge Kidney 41 0.193
8
HMM003 Hemimegalencephaly 45 0.171
9
P ANR002 Aniridia 64 0.126
10
P PHC003 Pheochromocytoma 71 0.115
11
ADN018 Adenoma 58 0.115
12
P SCL018 Scoliosis 55 0.115
13
HPT022 Hepatoblastoma 55 0.115
14
CRB009 Cerebritis 39 0.115
15
ANG062 Angioosteohypertrophic Syndrome 14 0.115
16
CPL012 Capillary Malformation of the Lower Lip, Lymphatic Malformation of Face and Neck, Asymmetry of Face and Limbs, and Partial/generalized Overgrowth 10 0.115
17
RHB003 Rhabdomyosarcoma 57 0.103
18
KLP010 Klippel-Trenaunay-Weber Syndrome 54 0.103
19
LPM005 Lipomatosis 47 0.103
20
VSC047 Vascular Malformation 45 0.103
21
WBR001 Weber Syndrome 41 0.103
22
P RNL014 Renal Cell Carcinoma 82 0.089
23
P HRT032 Heart Disease 75 0.089
24
P ADN016 Adenocarcinoma 69 0.089
25
P HYP060 Hyperinsulinism 58 0.089
26
CLR003 Clear Cell Adenocarcinoma 56 0.089
27
HYP077 Hypertrichosis 44 0.089
28
HMF009 Hemifacial Hyperplasia 32 0.089
29
P BRS047 Breast Cancer 100 0.073
30
P LKM002 Leukemia 71 0.073
31
P NRF002 Neurofibromatosis 71 0.073
32
P HPT021 Hepatitis 69 0.073
33
P HYD006 Hydrocephalus 66 0.073
34
P EPL164 Epilepsy 66 0.073
35
ART005 Arteriovenous Malformation 66 0.073
36
ACR007 Acromegaly 66 0.073
37
SRC014 Sarcoma 66 0.073
38
WLM007 Wilms Tumor Susceptibility-5 63 0.073
39
ACN011 Acne 62 0.073
40
P LYM025 Lymphedema 61 0.073
41
P RCK004 Rickets 61 0.073
42
P HMN010 Hemangioma 59 0.073
43
INC021 Incontinentia Pigmenti 59 0.073
44
ADR005 Adrenal Carcinoma 57 0.073
45
ACN002 Acanthosis Nigricans 57 0.073
46
P HYP613 Hypophosphatemic Rickets 57 0.073
47
P PLY006 Polydactyly 56 0.073
48
P EMB005 Embryonal Rhabdomyosarcoma 54 0.073
49
LYM022 Lymphangioma 54 0.073
50
NTH001 Netherton Syndrome 54 0.073
51
P HLL001 Hallermann-Streiff Syndrome 53 0.073
52
P OVR046 Ovarian Cyst 51 0.073
53
P PRC019 Precocious Puberty 51 0.073
54
c CNT075 Central Precocious Puberty 49 0.073
55
ADR008 Adrenal Adenoma 47 0.073
56
FLL008 Folliculitis 46 0.073
57
HMN009 Hemangioblastoma 45 0.073
58
RNL078 Renal Dysplasia 45 0.073
59
PRT019 Protein-Losing Enteropathy 42 0.073
60
IDP070 Idiopathic Scoliosis 41 0.073
61
CLV009 Clove Syndrome, Somatic 41 0.073
62
RTR010 Retroperitoneal Sarcoma 39 0.073
63
HMN016 Hemangioendothelioma 39 0.073
64
c CNG029 Congenital Mesoblastic Nephroma 37 0.073
65
c HRD009 Hereditary Wilms' Tumor 36 0.073
66
EMB002 Embryoma 34 0.073
67
P MSN006 Mesenchymoma 33 0.073
68
GGN002 Gigantism 32 0.073
69
THY043 Thymic Hyperplasia 32 0.073
70
CYS019 Cystathioninuria 29 0.073
71
MTN001 Metanephric Adenoma 28 0.073
72
c BNG012 Benign Mesenchymoma 28 0.073
73
P PRT063 Proteus-Like Syndrome 22 0.073
74
CHL076 Chilaiditi Syndrome 15 0.073
75
MSC081 Mosaic Trisomy 15 13 0.073
76
PHC005 Phacomatosis Pigmentokeratotica 12 0.073
77
HM3001 Hemi 3 Syndrome 9 0.073
78
P CSH001 Cushing's Syndrome 65 0.051
79
P KDN017 Kidney Cancer 65 0.051
80
HYP056 Hypoglycemia 61 0.051
81
EYD002 Eye Disease 61 0.051
82
OCL009 Ocular Cancer 59 0.051
83
ABL002 Ablepharon-Macrostomia Syndrome 57 0.051
84
c CWD006 Cowden Syndrome 1 57 0.051
85
ETH011 Ethylmalonic Encephalopathy 56 0.051
86
P FNC043 Fanconi Anemia, Complementation Group E 55 0.051
87
P RNL100 Renal Hypodysplasia/aplasia 1 53 0.051
88
WHM001 Whim Syndrome 53 0.051
89
ADR044 Adrenal Insufficiency, Congenital, with 46xy Sex Reversal, Partial or Complete 52 0.051
90
HND003 Hand-Foot-Uterus Syndrome 50 0.051
91
PRL032 Perlman Syndrome 50 0.051
92
URN009 Urinary System Disease 50 0.051
93
CSY001 C Syndrome 50 0.051
94
LRN003 Learning Disability 49 0.051
95
BRL010 Buruli Ulcer 48 0.051
96
VND001 Vein Disease 47 0.051
97
ACR041 Acromelic Frontonasal Dysostosis 45 0.051
98
MXD023 Mixed Cell Type Cancer 44 0.051
99
BRT030 Birth Defects 43 0.051
100
MGL023 Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome, Somatic 42 0.051
101
AYM001 Ayme-Gripp Syndrome 41 0.051
102
KRT063 Keratocystic Odontogenic Tumor 39 0.051
103
GLB003 Globe Disease 32 0.051
104
P HRT017 Heart Tumor 32 0.051
105
CVT001 Cavitary Optic Disc Anomalies 31 0.051
106
IRS003 Iris Disease 31 0.051
107
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 29 0.051
108
CYL001 Cayler Cardiofacial Syndrome 29 0.051
109
MNN028 Mononeuropathy of the Median Nerve, Mild 29 0.051
110
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 29 0.051
111
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 27 0.051
112
TTR012 Tetrasomy 9p 25 0.051
113
RHB020 Rhabdomyosarcoma, Somatic 24 0.051
114
HYP213 Hypomelanotic Disorder 21 0.051
115
UVL003 Uveal Diseases 18 0.051
116
ANT066 Anterior Cutaneous Nerve Entrapment Syndrome 17 0.051
117
P FML153 Familial Wilms Tumor 17 0.051
118
AND005 Androgen Insensitivity Syndrome, Mild 16 0.051
119
VSC050 Vascular Malformation, Primary Intraosseous 16 0.051
120
MXD009 Mixed Cell Type Kidney Wilms' Tumor 15 0.051
121
c RNL033 Renal Carcinoma, Familial 12 0.051
122
ANG035 Angiokeratoma Corporis Diffusum with Arteriovenous Fistulas 7 0.051
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