Search results for PHYH

74 hits were found for PHYH

# Family MCID Name MIFTS Score
1
RFS006 Refsum Disease, Classic 63 55.193
2
P RTN008 Retinitis Pigmentosa 80 23.153
3
FND002 Fundus Dystrophy 55 22.182
4
c ORF048 Orofacial Cleft 1 30 15.680
5
P RHZ001 Rhizomelic Chondrodysplasia Punctata 57 15.299
6
P CNR004 Cone-Rod Dystrophy 2 74 14.485
7
P ZLL001 Zellweger Syndrome 65 13.190
8
P ALZ034 Alzheimer Disease 87 12.220
9
PRX001 Peroxisomal Disease 46 11.350
10
P ICH004 Ichthyosis 56 11.166
11
c RHZ014 Rhizomelic Chondrodysplasia Punctata, Type 2 44 9.978
12
ICH001 Ichthyosis Vulgaris 53 9.978
13
c HRD026 Hereditary Ataxia 47 9.978
14
c PRX045 Peroxisome Biogenesis Disorder 1b 62 8.603
15
c RHZ011 Rhizomelic Chondrodysplasia Punctata, Type 1 53 8.244
16
P CHN044 Chondrodysplasia Punctata Syndrome 43 8.244
17
CLF004 Cleft Lip/palate 57 7.741
18
PRP018 Peripheral Nerve Schwannoma 23 7.055
19
c CNR007 Cone-Rod Dystrophy 6 52 7.055
20
PRX005 Peroxisomal Biogenesis Disorder 33 7.055
21
c RHZ004 Rhizomelic Chondrodysplasia Punctata, Type 3 42 7.055
22
c GCH017 Gaucher Disease, Type Iii 52 7.055
23
LBR036 Leber Plus Disease 66 7.055
24
ENC003 Encephalitozoonosis 23 7.055
25
HDG005 Hodgkin's Lymphoma, Mixed Cellularity 22 7.055
26
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 43 7.055
27
TST007 Testicular Infarct 21 7.055
28
c CHR094 Chronic Polyneuropathy 24 7.055
29
ALT002 Aleutian Mink Disease 27 7.055
30
PSD006 Pseudopterygium 29 7.055
31
NLL001 Null-Cell Leukemia 30 7.055
32
NRR001 Neuroretinitis 42 3.606
33
RTN023 Retinitis 46 3.606
34
RNL114 Renal Cell Carcinoma, Nonpapillary 80 3.335
35
CLR030 Clear Cell Renal Cell Carcinoma 54 3.335
36
P PLY019 Polyneuropathy 52 3.031
37
P NRP001 Neuropathy 60 1.940
38
P PRP019 Peripheral Nervous System Disease 58 1.940
39
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 1.815
40
P VTM027 Vitamin D-Dependent Rickets, Type 2a 53 1.601
41
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.372
42
c PRX050 Peroxisome Biogenesis Disorder 9b 31 1.372
43
CRD223 Cardiac Arrhythmia 63 1.188
44
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.188
45
c BRN108 Branchiootic Syndrome 1 62 1.188
46
SNS003 Sensory Peripheral Neuropathy 52 1.188
47
P NRB001 Neuroblastoma 66 0.970
48
P MLN007 Male Infertility 56 0.970
49
P INF032 Infertility 57 0.970
50
ZLL011 Zellweger Spectrum Disorder 45 0.970
51
c SPN398 Spinal Muscular Atrophy, Type Iv 44 0.686
52
P BRW001 Brown-Vialetto-Van Laere Syndrome 50 0.686
53
ATS010 Autosomal Recessive Disease 42 0.686
54
P HRD021 Hereditary Sensory Neuropathy 48 0.686
55
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 56 0.686
56
ALP012 Alpha-Methylacyl-Coa Racemase Deficiency 45 0.686
57
DWN001 Down Syndrome 70 0.686
58
P LKD001 Leukodystrophy 59 0.686
59
c ACT073 Acute Leukemia 58 0.686
60
RPD005 Rapidly Involuting Congenital Hemangioma 46 0.686
61
CLF001 Cleft Lip 53 0.686
62
FTT001 Fatty Liver Disease 62 0.686
63
P MVM001 Movement Disease 61 0.686
64
P LVR013 Liver Disease 69 0.686
65
HYP066 Hyperglycemia 61 0.686
66
P NGH001 Night Blindness 52 0.686
67
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.686
68
P CHR071 Charcot-Marie-Tooth Disease 64 0.686
69
TTH006 Tooth Disease 51 0.686
70
SQM006 Squamous Cell Carcinoma 60 0.686
72
P BRS047 Breast Cancer 98 0.573
73
P PNC035 Pancreatic Cancer 86 0.573
74
CLL010 Cellular Ependymoma 57 0.573
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