Search results for adnp

74 hits were found for adnp

# Family MCID Name MIFTS Score
1
HLS003 Helsmoortel-Van Der Aa Syndrome 47 21.016
3
P ATS364 Autism 70 4.352
4
c ATS007 Autism Spectrum Disorder 67 3.739
5
P HYP086 Hypothyroidism 69 2.944
6
CRP032 Corpus Callosum, Agenesis of 49 2.944
7
GRW007 Growth Hormone Deficiency 46 2.944
8
BLP004 Blepharophimosis 37 2.913
9
P SCH015 Schizophrenia 74 2.878
10
P CFF008 Coffin-Siris Syndrome 1 63 2.836
11
VSL002 Visual Epilepsy 59 2.137
12
c RRH009 Rare Hypothyroidism 24 2.137
13
P SPR120 Supranuclear Palsy, Progressive, 1 68 2.102
14
PCK003 Pick Disease of Brain 68 2.005
15
P PRV006 Pervasive Developmental Disorder 57 2.005
16
P FTL001 Fetal Alcohol Syndrome 57 2.005
17
FLT006 Floating-Harbor Syndrome 55 2.005
18
c FTL006 Fetal Alcohol Spectrum Disorder 43 2.005
19
c ATS203 Autosomal Dominant Non-Syndromic Intellectual Disability 36 2.005
20
P NNS031 Non-Syndromic Intellectual Disability 32 2.005
21
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.229
22
HDN002 Head Injury 46 0.132
23
P ALZ034 Alzheimer Disease 88 0.114
24
P HYP265 Hypotonia 43 0.114
25
P PHC003 Pheochromocytoma 71 0.093
26
ADR040 Adrenal Gland Pheochromocytoma 46 0.093
27
NNS045 Non-Specific Syndromic Intellectual Disability 31 0.093
28
P CLR023 Colorectal Cancer 99 0.066
29
P OVR042 Ovarian Cancer 88 0.066
30
P NNN008 Noonan Syndrome 1 76 0.066
31
P APL001 Aplastic Anemia 74 0.066
32
c SPN225 Spondyloarthropathy 1 73 0.066
33
P AMY004 Amyloidosis 70 0.066
34
P ANG001 Angelman Syndrome 69 0.066
35
P FRN006 Frontotemporal Dementia 68 0.066
36
c DPH024 Diaphragmatic Hernia, Congenital 63 0.066
37
P ANR048 Aniridia 1 63 0.066
38
c HYP794 Hyperoxaluria, Primary, Type I 63 0.066
39
ANR007 Anorexia Nervosa 63 0.066
40
P TRC086 Trichohepatoenteric Syndrome 1 62 0.066
41
MDD011 Mood Disorder 62 0.066
42
ACN002 Acanthosis Nigricans 60 0.066
43
P ALP009 Alopecia Areata 60 0.066
44
P SLP005 Sleep Disorder 59 0.066
45
P ALC033 Alcohol Use Disorder 58 0.066
46
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.066
47
CNS004 Constipation 58 0.066
48
ARS001 Aarskog-Scott Syndrome 57 0.066
49
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 56 0.066
50
ERY051 Erythroleukemia, Familial 56 0.066
51
MTH009 Mouth Disease 56 0.066
52
AGN016 Aging 56 0.066
53
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.066
54
P STR020 Strabismus 55 0.066
55
BLP046 Blepharophimosis, Ptosis, and Epicanthus Inversus 54 0.066
56
THR013 Thoracic Outlet Syndrome 54 0.066
57
c MLG077 Malignant Peripheral Nerve Sheath Tumor 54 0.066
58
P PTS002 Ptosis 53 0.066
59
P MSC003 Muscular Atrophy 52 0.066
60
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.066
61
BKR002 Baker-Gordon Syndrome 49 0.066
62
SVN002 Sveinsson Chorioretinal Atrophy 46 0.066
63
TRT001 Teratocarcinoma 45 0.066
64
INT276 Interatrial Communication 42 0.066
65
MCH006 Mechanical Strabismus 42 0.066
66
EPC005 Epicanthus 40 0.066
67
c ATR062 Atrial Septal Defect 1 39 0.066
68
FRS019 Farsightedness 38 0.066
69
CRB159 Cerebral Visual Impairment 35 0.066
70
ATX010 Ataxia Neuropathy Spectrum 34 0.066
71
ACT064 Acute Necrotizing Encephalitis 33 0.066
72
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.066
73
c PSD047 Pseudo-Turner Syndrome 21 0.066
74
BLD137 Blood Group--Ahonen 16 0.066
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