Search results for hemihypertrophy

105 hits were found for hemihypertrophy

# Family MCID Name MIFTS Score
1
HMH004 Hemihyperplasia, Isolated 43 7.836
2
HYP524 Hypoinsulinemic Hypoglycemia with Hemihypertrophy 18 6.078
3
P PRT008 Proteus Syndrome 67 5.525
4
HMF009 Hemifacial Hyperplasia 26 2.498
5
MCR030 Macrocephaly Mesodermal Hamartoma Spectrum 6 2.419
6
c WLM018 Wilms Tumor 5 49 0.236
7
c WLM011 Wilms Tumor 6 44 0.229
8
P BCK002 Beckwith-Wiedemann Syndrome 58 0.202
9
MDL009 Medullary Sponge Kidney 46 0.195
10
HMM003 Hemimegalencephaly 47 0.171
11
KLP010 Klippel-Trenaunay-Weber Syndrome 60 0.132
12
P ANR048 Aniridia 1 68 0.121
13
NVS017 Nevus, Epidermal 66 0.121
14
ANG062 Angioosteohypertrophic Syndrome 25 0.121
15
CPL012 Capillary Malformation of the Lower Lip, Lymphatic Malformation of Face and Neck, Asymmetry of Face and Limbs, and Partial/generalized Overgrowth 17 0.121
16
P PHC003 Pheochromocytoma 72 0.108
17
ADN018 Adenoma 63 0.108
18
P SCL018 Scoliosis 56 0.108
19
HPT022 Hepatoblastoma 55 0.108
20
CRB009 Cerebritis 41 0.108
21
P HRT032 Heart Disease 80 0.094
22
P RHB003 Rhabdomyosarcoma 61 0.094
23
P LPM005 Lipomatosis 50 0.094
24
WBR001 Weber Syndrome 40 0.094
25
P ADN016 Adenocarcinoma 71 0.076
26
c WLM013 Wilms Tumor 1 69 0.076
27
RNL114 Renal Cell Carcinoma, Nonpapillary 68 0.076
28
AGN016 Aging 65 0.076
29
ADR054 Adrenocortical Carcinoma, Hereditary 63 0.076
30
CLR003 Clear Cell Adenocarcinoma 57 0.076
31
HYP060 Hyperinsulinism 56 0.076
32
HYP077 Hypertrichosis 49 0.076
33
ADR004 Adrenal Cortical Adenocarcinoma 47 0.076
34
c HYP601 Hyperinsulinemic Hypoglycemia, Familial, 3 39 0.076
35
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 38 0.076
36
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 37 0.076
37
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 36 0.076
38
TTR012 Tetrasomy 9p 32 0.076
39
P BRS047 Breast Cancer 100 0.054
40
P LKM002 Leukemia 75 0.054
41
P HPT021 Hepatitis 75 0.054
42
NRF026 Neurofibromatosis, Type Iv, of Riccardi 72 0.054
43
ACR007 Acromegaly 70 0.054
44
P EPL164 Epilepsy 70 0.054
45
P KDN018 Kidney Disease 69 0.054
46
P HYD006 Hydrocephalus 68 0.054
47
SRC014 Sarcoma 68 0.054
48
P KDN017 Kidney Cancer 66 0.054
49
CRP001 Carpal Tunnel Syndrome 64 0.054
50
ART005 Arteriovenous Malformation 64 0.054
51
RCK004 Rickets 63 0.054
52
P LYM025 Lymphedema 63 0.054
53
HYP056 Hypoglycemia 62 0.054
54
P HMN010 Hemangioma 61 0.054
55
NTH001 Netherton Syndrome 60 0.054
56
ACN002 Acanthosis Nigricans 60 0.054
57
ADR005 Adrenal Carcinoma 59 0.054
58
P HLL001 Hallermann-Streiff Syndrome 58 0.054
59
URN009 Urinary System Disease 58 0.054
60
P PLY006 Polydactyly 57 0.054
61
INC021 Incontinentia Pigmenti 57 0.054
62
P RNL100 Renal Hypodysplasia/aplasia 1 57 0.054
63
HMN009 Hemangioblastoma 56 0.054
64
P EMB005 Embryonal Rhabdomyosarcoma 54 0.054
65
LYM022 Lymphangioma 53 0.054
66
c CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 53 0.054
67
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 53 0.054
68
c CNT075 Central Precocious Puberty 52 0.054
69
P OVR046 Ovarian Cyst 52 0.054
70
P PRC019 Precocious Puberty 52 0.054
71
ADR008 Adrenal Adenoma 51 0.054
72
FLL008 Folliculitis 50 0.054
73
HYP691 Hypomelanosis of Ito 49 0.054
74
RNL078 Renal Dysplasia 49 0.054
75
MGL038 Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome 48 0.054
76
P HRD009 Hereditary Wilms' Tumor 46 0.054
77
HMN016 Hemangioendothelioma 43 0.054
78
c CNG029 Congenital Mesoblastic Nephroma 43 0.054
79
IDP070 Idiopathic Scoliosis 42 0.054
80
c SPS219 Spastic Paraplegia 17, Autosomal Dominant 42 0.054
81
AYM001 Ayme-Gripp Syndrome 40 0.054
82
PRT019 Protein-Losing Enteropathy 40 0.054
83
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 39 0.054
84
RTR010 Retroperitoneal Sarcoma 39 0.054
85
THY043 Thymic Hyperplasia 38 0.054
86
DLT018 Dilution, Pigmentary 37 0.054
87
P MSN006 Mesenchymoma 37 0.054
88
CYL001 Cayler Cardiofacial Syndrome 36 0.054
89
GGN002 Gigantism 36 0.054
90
ASC009 Ascites, Chylous 35 0.054
91
MNN028 Mononeuropathy of the Median Nerve, Mild 35 0.054
92
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.054
93
IRS003 Iris Disease 31 0.054
94
MTN001 Metanephric Adenoma 31 0.054
95
CYS019 Cystathioninuria 30 0.054
96
VSC050 Vascular Malformation, Primary Intraosseous 27 0.054
97
c PRT063 Proteus-Like Syndrome 26 0.054
98
c BNG012 Benign Mesenchymoma 24 0.054
99
UVL003 Uveal Diseases 23 0.054
100
TNR001 Tenorio Syndrome 21 0.054
101
CHL076 Chilaiditi Syndrome 18 0.054
102
MSC081 Mosaic Trisomy 15 18 0.054
103
PHC005 Phacomatosis Pigmentokeratotica 14 0.054
104
ANG035 Angiokeratoma Corporis Diffusum with Arteriovenous Fistulas 9 0.054
105
HM3001 Hemi 3 Syndrome 9 0.054
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