Search results for ADNP

71 hits were found for ADNP

# Family MCID Name MIFTS Score
1
HLS003 Helsmoortel-Van Der Aa Syndrome 42 21.054
3
P ATS364 Autism 65 4.397
4
c ATS007 Autism Spectrum Disorder 67 3.747
5
P HYP086 Hypothyroidism 68 2.964
6
GRW007 Growth Hormone Deficiency 43 2.964
7
P SCH015 Schizophrenia 75 2.932
8
BLP004 Blepharophimosis 37 2.932
9
P CFF008 Coffin-Siris Syndrome 1 62 2.853
10
VSL002 Visual Epilepsy 58 2.152
11
CRP032 Corpus Callosum, Agenesis of 49 2.152
12
c RRH009 Rare Hypothyroidism 23 2.152
13
P SPR120 Supranuclear Palsy, Progressive, 1 68 2.116
14
PCK003 Pick Disease of Brain 68 2.018
15
P PRV006 Pervasive Developmental Disorder 57 2.018
16
P FTL001 Fetal Alcohol Syndrome 55 2.018
17
CRB151 Cerebral Creatine Deficiency Syndrome 1 48 2.018
18
c FTL006 Fetal Alcohol Spectrum Disorder 42 2.018
19
c ATS203 Autosomal Dominant Non-Syndromic Intellectual Disability 36 2.018
20
P NNS031 Non-Syndromic Intellectual Disability 28 2.018
21
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.223
22
HDN002 Head Injury 45 0.135
23
P ALZ034 Alzheimer Disease 88 0.116
24
P HYP265 Hypotonia 42 0.116
25
P PHC003 Pheochromocytoma 71 0.095
26
ADR040 Adrenal Gland Pheochromocytoma 46 0.095
27
NNS045 Non-Specific Syndromic Intellectual Disability 28 0.095
28
P CLR023 Colorectal Cancer 98 0.067
29
P OVR042 Ovarian Cancer 89 0.067
30
P NNN008 Noonan Syndrome 1 76 0.067
31
P APL001 Aplastic Anemia 74 0.067
32
c SPN225 Spondyloarthropathy 1 73 0.067
33
P AMY004 Amyloidosis 70 0.067
34
P FRN006 Frontotemporal Dementia 70 0.067
35
P ANG001 Angelman Syndrome 67 0.067
36
P ANR048 Aniridia 1 63 0.067
37
ANR007 Anorexia Nervosa 63 0.067
38
MDD011 Mood Disorder 62 0.067
39
ACN002 Acanthosis Nigricans 60 0.067
40
P ALP009 Alopecia Areata 60 0.067
41
P SLP005 Sleep Disorder 59 0.067
42
P TRC086 Trichohepatoenteric Syndrome 1 59 0.067
43
P ALC033 Alcohol Use Disorder 58 0.067
44
CNS004 Constipation 57 0.067
45
ARS001 Aarskog-Scott Syndrome 57 0.067
46
P STR020 Strabismus 56 0.067
47
ERY051 Erythroleukemia, Familial 56 0.067
48
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.067
49
AGN016 Aging 56 0.067
50
MTH009 Mouth Disease 56 0.067
51
BLP046 Blepharophimosis, Ptosis, and Epicanthus Inversus 55 0.067
52
c MLG077 Malignant Peripheral Nerve Sheath Tumor 54 0.067
53
THR013 Thoracic Outlet Syndrome 53 0.067
54
P PTS002 Ptosis 52 0.067
55
P MSC003 Muscular Atrophy 52 0.067
56
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.067
57
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 50 0.067
58
c HYP794 Hyperoxaluria, Primary, Type I 48 0.067
59
TRT001 Teratocarcinoma 46 0.067
60
EPC005 Epicanthus 43 0.067
61
INT276 Interatrial Communication 42 0.067
62
c ATR062 Atrial Septal Defect 1 40 0.067
63
BKR002 Baker-Gordon Syndrome 40 0.067
64
MCH006 Mechanical Strabismus 39 0.067
65
FRS019 Farsightedness 38 0.067
66
ATX010 Ataxia Neuropathy Spectrum 38 0.067
67
SVN002 Sveinsson Chorioretinal Atrophy 36 0.067
68
CRB159 Cerebral Visual Impairment 35 0.067
69
ACT064 Acute Necrotizing Encephalitis 32 0.067
70
c PSD047 Pseudo-Turner Syndrome 21 0.067
71
BLD137 Blood Group--Ahonen 19 0.067
Content
Loading form....