Search results for arl2

26 hits were found for arl2

# Family MCID Name MIFTS Score
1
P RTN008 Retinitis Pigmentosa 77 3.423
2
c HRD010 Hereditary Spastic Paraplegia 66 3.371
3
c RTN162 Retinitis Pigmentosa 2 43 3.371
4
c DFN243 Deafness, Autosomal Recessive 88 24 2.452
5
P JBR020 Joubert Syndrome 1 72 2.383
6
HYP134 Hypoparathyroidism-Retardation-Dysmorphism Syndrome 52 2.383
7
c RTN152 Retinitis Pigmentosa 66 34 2.383
8
P RTN016 Retinal Degeneration 53 0.143
9
CRV035 Cervical Cancer 76 0.083
10
SVR004 Severe Combined Immunodeficiency 73 0.083
11
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.083
12
P GLM045 Glioma 63 0.083
13
c BRN108 Branchiootic Syndrome 1 61 0.083
14
P CTR002 Cataract 60 0.083
15
P BRS044 Breast Adenocarcinoma 59 0.083
16
c OPT053 Optic Atrophy 1 54 0.083
17
MCR141 Mucormycosis 51 0.083
18
SPP010 Suppressor of Tumorigenicity 3 51 0.083
19
P OVR082 Overgrowth Syndrome 50 0.083
20
c NNS007 Nonsyndromic Deafness 47 0.083
21
RTN023 Retinitis 46 0.083
22
GLL048 Glial Tumor 45 0.083
23
c NPH031 Nephronophthisis 3 44 0.083
24
NRR001 Neuroretinitis 43 0.083
25
P CND005 Cone Dystrophy 41 0.083
26
ATS252 Autosomal Recessive Non-Syndromic Sensorineural Deafness Type Dfnb 31 0.083
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