Search results for PHOX2B

46 hits were found for PHOX2B

# Family MCID Name MIFTS Score
1
CNT097 Central Hypoventilation Syndrome, Congenital 57 6.296
2
P NRB001 Neuroblastoma 71 5.669
3
c NRB015 Neuroblastoma 2 32 4.593
4
P SDD001 Sudden Infant Death Syndrome 60 4.523
5
LRN003 Learning Disability 46 3.477
6
P HRS035 Hirschsprung Disease 1 58 3.438
7
HRS003 Hirschsprung Disease Ganglioneuroblastoma 17 3.009
8
PRP019 Peripheral Nervous System Disease 53 2.807
9
CLN019 Colonic Disease 51 2.807
10
ATN002 Autonomic Nervous System Disease 48 2.807
11
PRP021 Peripheral Nervous System Neoplasm 48 2.807
12
MGC001 Megacolon 46 2.807
13
ATN003 Autonomic Nervous System Neoplasm 41 2.807
14
c HRD009 Hereditary Wilms' Tumor 40 2.807
15
EXT022 Exotropia 39 2.807
16
P NRB002 Neuroblastoma, Susceptibility 25 2.044
17
c PHX002 Phox2b-Related Neuroblastoma, Susceptibility 3 2.044
18
NRN002 Neuronitis 39 0.202
19
P SLP006 Sleep Apnea 60 0.143
20
c CNT015 Central Sleep Apnea 43 0.124
21
CRH001 Crohn's Disease 73 0.101
22
P RSP003 Respiratory Failure 68 0.101
23
RSP006 Respiratory System Disease 60 0.101
24
CHL071 Child Syndrome 59 0.101
25
KDS001 Kid Syndrome 57 0.101
26
ADL002 Adult Syndrome 57 0.101
27
SLP005 Sleep Disorder 54 0.101
28
ATN005 Autonomic Dysfunction 45 0.101
29
c PLM022 Pulmonary Valve Insufficiency 37 0.101
30
P PLM037 Pulmonary Hypertension 77 0.071
31
CNG034 Congestive Heart Failure 70 0.071
32
OBS061 Obstructive Sleep Apnea 65 0.071
33
P EPL164 Epilepsy 65 0.071
34
LNG099 Lung Disease 61 0.071
35
WLL006 Wells Syndrome 58 0.071
36
GDS001 Good Syndrome 46 0.071
37
HMS001 Hemosiderosis 44 0.071
38
P PLM085 Pulmonary Hemosiderosis 44 0.071
39
RPR002 Reproductive System Disease 43 0.071
40
P HYP729 Hypersensitivity Reaction Disease 43 0.071
41
IRN002 Iron Metabolism Disease 42 0.071
42
P FML187 Familial Hypertension 37 0.071
43
RDN001 Reading Disorder 36 0.071
44
NNT004 Neonatal Respiratory Failure 35 0.071
45
PLM124 Pulmonary Hypertension, Neonatal 27 0.071
46
INF043 Infantile Apnea 20 0.071
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