Search results for taf6

48 hits were found for taf6

# Family MCID Name MIFTS Score
1
ALZ044 Alazami-Yuan Syndrome 23 37.005
2
P CRN015 Cornelia De Lange Syndrome 67 27.356
3
c CRN139 Cornelia De Lange Syndrome 1 61 18.702
4
P SYN057 Syndromic Intellectual Disability 37 18.525
5
P MCR010 Microcephaly 59 12.136
6
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 10.120
7
KBG001 Kbg Syndrome 54 8.581
8
GLB002 Glioblastoma 67 1.208
9
BRN028 Brain Cancer 73 1.208
10
GLM045 Glioma 62 1.208
11
GLL048 Glial Tumor 52 1.208
12
WDM004 Wiedemann-Steiner Syndrome 48 1.158
13
P BRS047 Breast Cancer 97 0.779
14
P LKM062 Leukemia, Acute Lymphoblastic 69 0.551
15
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.551
16
P PNC035 Pancreatic Cancer 86 0.551
17
HLX001 Helix Syndrome 47 0.250
18
c PRM089 Premature Ovarian Failure 3 24 0.176
19
c MLT139 Multiple Mitochondrial Dysfunctions Syndrome 4 35 0.176
20
DVL022 Developmental Delay with Short Stature, Dysmorphic Facial Features, and Sparse Hair 29 0.176
21
ALK024 Alkuraya-Kucinskas Syndrome 45 0.176
22
c MNT339 Mental Retardation, Autosomal Recessive 66 22 0.176
23
NRL023 Neurologic, Endocrine, and Pancreatic Disease, Multisystem, Infantile-Onset 33 0.176
24
c DVL064 Developmental and Epileptic Encephalopathy 38 26 0.176
25
c PNT042 Pontocerebellar Hypoplasia, Type 2f 21 0.176
26
c GLL046 Galloway-Mowat Syndrome 7 24 0.176
27
c MLT179 Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 4 26 0.176
28
NRD099 Neurodevelopmental Disorder and Structural Brain Anomalies with or Without Seizures and Spasticity 24 0.176
29
ATS010 Autosomal Recessive Disease 42 0.176
30
P MLT027 Multiple Mitochondrial Dysfunctions Syndrome 37 0.176
31
P HYP714 Hypotonia, Infantile, with Psychomotor Retardation and Characteristic Facies 3 31 0.176
32
c CRB136 Cerebellar Ataxia, Mental Retardation, and Dysequilibrium Syndrome 2 28 0.176
33
c MLG147 Malignant Hyperthermia 1 47 0.176
34
c DVL040 Developmental and Epileptic Encephalopathy 12 37 0.176
35
c PNT034 Pontocerebellar Hypoplasia, Type 2e 52 0.176
36
c CRN209 Cornelia De Lange Syndrome 5 38 0.176
37
SRC014 Sarcoma 64 0.176
38
P PRD006 Prader-Willi Syndrome 60 0.176
39
P EPL164 Epilepsy 70 0.176
40
NRD046 Neurodevelopmental Disorder with Microcephaly, Cataracts, and Renal Abnormalities 21 0.176
41
c MLG084 Malignant Fibrous Histiocytoma 62 0.176
42
P LKM002 Leukemia 66 0.176
43
SPN035 Spindle Cell Sarcoma 51 0.176
44
P FBR003 Fibrous Histiocytoma 43 0.176
45
P SZR006 Seizure Disorder 69 0.176
47
MLG086 Malignant Hyperthermia Susceptibility 39 0.176
48
DSR002 Disorders of Intracellular Cobalamin Metabolism 30 0.176
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