Search results for gnb1

Showing 25 of 174 hits for gnb1
# Family MCID Name MIFTS Score
1
c INT453 Intellectual Developmental Disorder, Autosomal Dominant 42 36 45.048
2
HYP265 Hypotonia 46 30.498
3
GNB001 Gnb1 Encephalopathy 7 24.951
4
MYL009 Myelodysplastic Syndrome 64 24.175
5
P DYS154 Dystonia 66 23.407
6
P LKM062 Leukemia, Acute Lymphoblastic 69 19.775
7
P STR020 Strabismus 57 19.343
8
CRB037 Cerebral Palsy 66 17.853
9
P RTN008 Retinitis Pigmentosa 80 14.425
10
c ATS007 Autism Spectrum Disorder 70 13.291
11
P MCR010 Microcephaly 59 12.455
12
CRB159 Cerebral Visual Impairment 44 10.820
13
CLF027 Cleft Palate, Isolated 63 9.950
14
WST001 West Syndrome 64 9.433
15
P HYP086 Hypothyroidism 68 9.260
16
CHR222 Chromosome 1p36 Deletion Syndrome 48 8.167
17
P CNR004 Cone-Rod Dystrophy 2 78 7.976
18
c OPT060 Optic Atrophy 8 25 7.650
19
c NGH024 Night Blindness, Congenital Stationary, Type 1h 34 7.650
20
c CHR035 Chronic Dacryoadenitis 16 7.650
21
P ENC018 Encephalopathy 64 2.911
22
MST024 Mastocytosis, Cutaneous 65 2.730
23
P MST009 Mastocytosis 66 2.730
24
SGC002 Sgce Myoclonus-Dystonia 23 2.049
25
VSL002 Visual Epilepsy 47 2.034
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