Search results for cep63

Showing 25 of 52 hits for cep63
# Family MCID Name MIFTS Score
1
c SCK032 Seckel Syndrome 6 30 37.981
2
c PRM031 Primary Autosomal Recessive Microcephaly 51 18.233
3
c MYP119 Myopathy, Myofibrillar, 7 35 16.209
4
P MCR010 Microcephaly 59 15.909
5
P SCK004 Seckel Syndrome 55 14.859
6
P DYS005 Dyslexia 40 11.979
7
P CNR004 Cone-Rod Dystrophy 2 78 10.819
8
c PRM212 Primary Microcephaly 39 9.498
9
ISL014 Isolated Growth Hormone Deficiency, Type Ia 58 8.707
10
P MCR258 Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii 56 8.633
11
c HRD010 Hereditary Spastic Paraplegia 68 8.558
12
c MCR239 Microcephaly 5, Primary, Autosomal Recessive 49 7.827
13
P MRG008 Meier-Gorlin Syndrome 1 57 7.650
14
c BRN140 Brain Small Vessel Disease 2 39 7.650
15
P MSC022 Mosaic Variegated Aneuploidy Syndrome 52 7.650
16
c CNG031 Congenital Nervous System Abnormality 32 7.650
17
RDN001 Reading Disorder 44 7.650
18
c THY109 Thyroid Cancer, Nonmedullary, 1 57 2.024
19
THY029 Thyroid Carcinoma 52 2.024
20
P BLD134 Bladder Cancer 74 1.671
21
PPL002 Papillary Carcinoma 45 1.491
22
P NRB001 Neuroblastoma 62 1.274
23
P MLN007 Male Infertility 59 1.202
24
P INF032 Infertility 59 1.202
25
LRN003 Learning Disability 45 1.160
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