Search results for golga2

45 hits were found for golga2

# Family MCID Name MIFTS Score
1
P LNG028 Long Qt Syndrome 63 11.636
2
P ACH011 Achondrogenesis 53 8.411
3
DYG001 Dyggve-Melchior-Clausen Disease 47 8.228
4
CHN016 Cohen Syndrome 59 8.228
5
P VHW001 Vohwinkel Syndrome 50 8.228
6
c MCL016 Mucolipidosis Iii Gamma 49 8.228
7
P SMT022 Smith-Mccort Dysplasia 1 47 8.228
8
P RTN008 Retinitis Pigmentosa 79 8.228
9
ENC039 Encephalopathy, Familial, with Neuroserpin Inclusion Bodies 46 8.228
10
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 1.261
11
P MCR010 Microcephaly 59 1.261
12
P MSC005 Muscular Dystrophy 66 1.261
13
P LNG021 Lung Occult Small Cell Carcinoma 20 1.215
14
LNG019 Lung Combined Type Small Cell Carcinoma 34 1.215
15
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 1.215
16
P BRS047 Breast Cancer 97 0.811
17
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.573
18
P PNC035 Pancreatic Cancer 87 0.573
19
EPD052 Epidermolysis Bullosa Simplex Superficialis 17 0.449
20
TBL029 Tubulin, Beta 28 0.317
21
c ATS007 Autism Spectrum Disorder 71 0.183
22
P PRS040 Prostate Cancer 95 0.183
23
c CRB094 Cerebral Cavernous Malformations 3 41 0.183
24
c DVL100 Developmental and Epileptic Encephalopathy 76 33 0.183
25
INT376 Intellectual Developmental Disorder with Poor Growth and with or Without Seizures or Ataxia 17 0.183
26
ATS010 Autosomal Recessive Disease 42 0.183
27
NRD046 Neurodevelopmental Disorder with Microcephaly, Cataracts, and Renal Abnormalities 21 0.183
28
c DVL085 Developmental and Epileptic Encephalopathy 61 23 0.183
29
MTB009 Metabolic Crises, Recurrent, with Variable Encephalomyopathic Features and Neurologic Regression 21 0.183
30
c DVL104 Developmental and Epileptic Encephalopathy 81 24 0.183
31
c CLR142 Ciliary Dyskinesia, Primary, 42 22 0.183
32
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.183
33
P CRB048 Cerebral Cavernous Malformations 63 0.183
34
c SPN272 Spinocerebellar Ataxia, Autosomal Recessive 15 30 0.183
35
P DNG005 Dengue Virus 55 0.183
36
P HNT016 Huntington Disease 73 0.183
37
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.183
38
P PLY014 Polycystic Kidney Disease 71 0.183
39
c HRD010 Hereditary Spastic Paraplegia 65 0.183
40
GLB002 Glioblastoma 67 0.183
41
PRP016 Paraplegia 52 0.183
42
P OPT006 Optic Nerve Disease 57 0.183
43
P GST044 Gastritis 55 0.183
44
c ATS347 Autosomal Dominant Polycystic Kidney Disease 64 0.183
45
CVR010 Cavernous Malformation 29 0.183
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