Search results for frmpd4

56 hits were found for frmpd4

# Family MCID Name MIFTS Score
1
c MNT267 Mental Retardation, X-Linked 104 25 44.205
2
VRG001 Variegate Porphyria 55 9.429
3
P NNS032 Non-Syndromic X-Linked Intellectual Disability 46 9.183
4
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 3.703
5
c ATS268 Autism X-Linked 4 24 2.363
6
DSS008 Disease of Mental Health 74 1.671
7
P SCH015 Schizophrenia 74 1.385
8
c MSM022 Mismatch Repair Cancer Syndrome 1 69 1.268
9
c GLM043 Glioma Susceptibility 9 30 1.268
10
c GLM047 Glioma Susceptibility 3 32 1.268
11
c GLM025 Glioma Susceptibility 2 29 1.268
12
P GLM040 Glioma Susceptibility 1 70 1.268
13
P OLG002 Oligodendroglioma 66 1.268
14
MNN043 Meningioma, Familial 79 1.268
15
GLM045 Glioma 62 1.268
16
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.982
17
LNG019 Lung Combined Type Small Cell Carcinoma 32 0.982
18
P LNG021 Lung Occult Small Cell Carcinoma 20 0.982
19
c CLR087 Colorectal Cancer 12 34 0.802
20
GST103 Gastric Cancer, Hereditary Diffuse 68 0.802
21
SML009 Small Intestine Adenocarcinoma 57 0.802
22
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 60 0.802
23
P PNC035 Pancreatic Cancer 86 0.642
24
CLN015 Colon Adenocarcinoma 64 0.567
25
CHR020 Chronic Interstitial Cystitis 36 0.471
26
P JBR020 Joubert Syndrome 1 74 0.180
27
c PRX059 Peroxisome Biogenesis Disorder 1a 56 0.180
28
WLS003 Wilson-Turner X-Linked Mental Retardation Syndrome 47 0.180
29
RYN006 Raynaud-Claes Syndrome 29 0.180
30
MSS001 Masa Syndrome 60 0.180
31
CRP035 Corpus Callosum, Partial Agenesis of, X-Linked 38 0.180
32
c ACR088 Aicardi-Goutieres Syndrome 3 39 0.180
33
NRD099 Neurodevelopmental Disorder and Structural Brain Anomalies with or Without Seizures and Spasticity 24 0.180
34
WST001 West Syndrome 64 0.180
35
c HYD019 Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius 48 0.180
36
c MSC047 Muscular Dystrophy-Dystroglycanopathy , Type a, 1 55 0.180
37
P MCK013 Meckel Syndrome, Type 1 64 0.180
38
P ERL057 Early Infantile Epileptic Encephalopathy 61 0.180
39
P SLL003 Salla Disease 45 0.180
40
c SPN101 Spinocerebellar Ataxia 29 58 0.180
41
c MNT274 Mental Retardation, X-Linked 105 18 0.180
42
MNT306 Mental Retardation, X-Linked, Syndromic, Houge Type 19 0.180
43
c MNT196 Mental Retardation, X-Linked 92 18 0.180
44
INF159 Infantile Sialic Acid Storage Disease 41 0.180
45
RLN001 Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked 23 0.180
46
c DVL029 Developmental and Epileptic Encephalopathy 2 46 0.180
47
TNN015 Tonne-Kalscheuer Syndrome 30 0.180
48
c MNT289 Mental Retardation, X-Linked 103 21 0.180
49
WLK001 Walker-Warburg Syndrome 62 0.180
50
P NPH005 Nephronophthisis 59 0.180
51
P BCL017 B-Cell Lymphoma 57 0.180
52
P FRS004 Free Sialic Acid Storage Disorders 41 0.180
53
P SCK005 Sickle Cell Disease 56 0.180
54
P ZLL001 Zellweger Syndrome 65 0.180
55
HYD048 Hydrocephalus with Stenosis of the Aqueduct of Sylvius 37 0.180
56
c JVN041 Juvenile Nephronophthisis 45 0.180
Content
Loading form....