Search results for phox2b

75 hits were found for phox2b

# Family MCID Name MIFTS Score
1
CNT097 Central Hypoventilation Syndrome, Congenital 70 8.513
2
c NRB015 Neuroblastoma 2 26 5.563
3
P NRB010 Neuroblastoma 1 66 4.712
4
SDD001 Sudden Infant Death Syndrome 61 4.557
5
HRS003 Hirschsprung Disease Ganglioneuroblastoma 16 4.157
6
P HRS035 Hirschsprung Disease 1 65 4.065
7
GNG008 Ganglioneuroblastoma 47 3.588
8
LRN003 Learning Disability 51 3.506
9
P PRP019 Peripheral Nervous System Disease 64 2.835
10
P ATN002 Autonomic Nervous System Disease 52 2.835
11
MGC001 Megacolon 47 2.835
12
P PRP021 Peripheral Nervous System Neoplasm 45 2.835
13
EXT022 Exotropia 41 2.835
14
P ATN003 Autonomic Nervous System Neoplasm 31 2.835
15
c ATN017 Autonomic Nervous System Benign Neoplasm 20 2.835
16
c PRP105 Peripheral Nervous System Benign Neoplasm 19 2.835
17
CLN019 Colonic Disease 55 2.004
18
INH023 Inherited Cancer-Predisposing Syndrome 46 0.458
19
P SLP006 Sleep Apnea 71 0.191
20
ATN005 Autonomic Dysfunction 48 0.191
21
P RSP003 Respiratory Failure 75 0.180
22
CYN002 Cyanosis, Transient Neonatal 45 0.142
23
c CNT015 Central Sleep Apnea 48 0.127
24
HLX001 Helix Syndrome 46 0.110
25
P HRT032 Heart Disease 78 0.090
26
CRH001 Crohn's Disease 75 0.090
27
P PHC003 Pheochromocytoma 71 0.090
28
EWN003 Ewing Sarcoma 69 0.090
29
CRN036 Craniopharyngioma 65 0.090
30
P RHB003 Rhabdomyosarcoma 62 0.090
31
LNG099 Lung Disease 62 0.090
32
c HYP595 Hypertension, Essential 87 0.064
33
P MDL005 Medulloblastoma 78 0.064
34
ULC004 Ulcerative Colitis 75 0.064
35
SVR004 Severe Combined Immunodeficiency 74 0.064
36
P RTN024 Retinoblastoma 74 0.064
37
c NRF024 Neurofibromatosis, Type I 72 0.064
38
P PLM037 Pulmonary Hypertension 69 0.064
39
CNG034 Congestive Heart Failure 69 0.064
40
P LNG028 Long Qt Syndrome 68 0.064
41
GST092 Gastroesophageal Reflux 68 0.064
42
c INF071 Inflammatory Bowel Disease 1 66 0.064
43
APN008 Apnea, Obstructive Sleep 64 0.064
44
c WLM018 Wilms Tumor 5 63 0.064
45
P MYP004 Myopathy 63 0.064
46
NRM005 Neuromuscular Disease 62 0.064
47
P WRD001 Waardenburg's Syndrome 60 0.064
48
BRN002 Bronchiolitis 60 0.064
49
TMR010 Tumor Predisposition Syndrome 58 0.064
50
P SLP005 Sleep Disorder 58 0.064
51
P INF037 Inflammatory Bowel Disease 57 0.064
52
EMB004 Embryonal Carcinoma 57 0.064
53
P PLY018 Polycythemia 56 0.064
54
HMS001 Hemosiderosis 54 0.064
55
P PTS002 Ptosis 53 0.064
56
P PRG013 Paraganglioma 53 0.064
57
GNG005 Gangliocytoma 52 0.064
58
GNG002 Ganglioneuroma 52 0.064
59
AZS001 Azoospermia 51 0.064
60
ADR040 Adrenal Gland Pheochromocytoma 51 0.064
61
PLY012 Polyhydramnios 48 0.064
62
TKL001 Tukel Syndrome 47 0.064
63
c FML008 Familial Retinoblastoma 46 0.064
64
ATX019 Ataxia with Vitamin E Deficiency 46 0.064
65
DVR002 Diverticulitis 44 0.064
66
P MJR007 Major Affective Disorder 1 44 0.064
67
P PLM085 Pulmonary Hemosiderosis 43 0.064
68
P DYS021 Dysautonomia 41 0.064
69
c MCK031 Meckel Syndrome, Type 2 41 0.064
70
DFF012 Differentiating Neuroblastoma 32 0.064
71
NRL008 Neural Crest Tumor 26 0.064
72
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.064
73
ANS021 Anisocoria 25 0.064
74
c HRS034 Hirschsprung Disease 3 23 0.064
75
c INF074 Inflammatory Bowel Disease 15 17 0.064
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