Search results for PHOX2B

35 hits were found for PHOX2B

# Family MCID Name MIFTS Score
1
CNT097 Central Hypoventilation Syndrome, Congenital 65 7.341
2
P NRB001 Neuroblastoma 73 5.849
3
c NRB015 Neuroblastoma 2 18 5.178
4
SDD001 Sudden Infant Death Syndrome 61 4.656
5
P HRS035 Hirschsprung Disease 1 64 3.676
6
LRN003 Learning Disability 49 3.578
7
HRS003 Hirschsprung Disease Ganglioneuroblastoma 17 3.104
8
CLN019 Colonic Disease 55 2.888
9
PRP019 Peripheral Nervous System Disease 53 2.888
10
PRP021 Peripheral Nervous System Neoplasm 53 2.888
11
ATN002 Autonomic Nervous System Disease 51 2.888
12
MGC001 Megacolon 50 2.888
13
P HRD009 Hereditary Wilms' Tumor 46 2.888
14
EXT022 Exotropia 41 2.888
15
ATN003 Autonomic Nervous System Neoplasm 32 2.888
16
NRN002 Neuronitis 43 0.216
17
P SLP006 Sleep Apnea 65 0.153
18
c CNT015 Central Sleep Apnea 45 0.133
19
CRH001 Crohn's Disease 80 0.108
20
P RSP003 Respiratory Failure 71 0.108
21
SLP005 Sleep Disorder 59 0.108
22
ATN005 Autonomic Dysfunction 51 0.108
23
c PLM022 Pulmonary Valve Insufficiency 38 0.108
24
c MLT151 Multiple Mitochondrial Dysfunctions Syndrome 5 36 0.108
25
P PLM037 Pulmonary Hypertension 79 0.076
26
CNG034 Congestive Heart Failure 74 0.076
27
P EPL164 Epilepsy 70 0.076
28
LNG099 Lung Disease 67 0.076
29
APN008 Apnea, Obstructive Sleep 67 0.076
30
HMS001 Hemosiderosis 50 0.076
31
P PLM085 Pulmonary Hemosiderosis 48 0.076
32
PLY112 Polyarteritis Nodosa, Childhood-Onset 39 0.076
33
PPL059 Popliteal Pterygium Syndrome, Lethal Type 37 0.076
34
APN007 Apnea, Central Sleep 18 0.076
35
HMS004 Hemosiderosis, Pulmonary, with Deficiency of Gamma-a Globulin 11 0.076
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