Search results for hypotrichosis, localized, autosomal recessive, 3

81 hits were found for hypotrichosis, localized, autosomal recessive, 3

# Family MCID Name MIFTS Score
1
c HYP559 Hypotrichosis 8 34 5.759
2
P HYP087 Hypotrichosis 48 0.418
3
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.248
4
c BLD140 Blood Group, I System 37 0.242
5
SKN016 Skin Disease 68 0.226
6
P ANR048 Aniridia 1 68 0.224
7
RTN023 Retinitis 52 0.219
8
ANR038 Anorexia Nervosa 1 21 0.218
9
BLD137 Blood Group--Ahonen 17 0.218
10
AGN016 Aging 65 0.193
11
ALR002 Al-Raqad Syndrome 30 0.189
12
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.156
13
P LYM118 Lymphoma 71 0.154
14
P ICH004 Ichthyosis 54 0.150
15
P THY032 Thyroiditis 56 0.149
16
P EPL164 Epilepsy 70 0.144
17
c BRN108 Branchiootic Syndrome 1 47 0.141
18
P PRD008 Periodontitis 67 0.141
19
P ALP008 Alopecia 56 0.140
20
ALP046 Alport Syndrome, X-Linked 74 0.139
21
c LBR014 Leber Congenital Amaurosis 4 48 0.137
22
P CTR002 Cataract 60 0.134
23
P LVR013 Liver Disease 76 0.130
24
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.127
25
P LYM025 Lymphedema 63 0.113
26
ECT006 Ectodermal Dysplasia 57 0.113
27
SNS001 Sensorineural Hearing Loss 59 0.108
28
P INF032 Infertility 59 0.105
29
DRM006 Dermatitis 67 0.104
30
c BSL007 Basal Cell Carcinoma 66 0.102
31
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.100
32
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 62 0.100
33
MCS002 Mucositis 61 0.100
34
P RTN016 Retinal Degeneration 56 0.092
35
KRT009 Keratosis 53 0.091
36
P GLM007 Glomerulonephritis 61 0.088
37
c BSL024 Basal Cell Carcinoma 1 42 0.084
38
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.083
39
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 33 0.083
40
MST019 Mastoiditis 33 0.081
41
STR020 Strabismus 55 0.073
42
P BRC006 Brachydactyly 57 0.073
43
P DRM053 Dermatitis, Atopic 68 0.071
44
MCR013 Microphthalmia 61 0.071
45
P FNC043 Fanconi Anemia, Complementation Group E 52 0.070
46
c MCL042 Macular Degeneration, Age-Related, 1 79 0.069
47
NTH001 Netherton Syndrome 60 0.066
48
CLF001 Cleft Lip 54 0.065
49
P HMN010 Hemangioma 61 0.065
50
ADP007 Adie Pupil 41 0.064
51
P TRC086 Trichohepatoenteric Syndrome 1 54 0.064
52
GRW007 Growth Hormone Deficiency 52 0.063
53
P HLP001 Holoprosencephaly 67 0.062
54
ANH002 Anhidrosis 45 0.062
55
INN002 Inner Ear Disease 52 0.062
56
DWN001 Down Syndrome 70 0.061
57
LPD016 Lipoid Proteinosis of Urbach and Wiethe 54 0.061
58
CLF027 Cleft Palate, Isolated 61 0.061
59
CNG008 Congenital Ichthyosiform Erythroderma 61 0.060
60
c HMC039 Hemochromatosis, Type 1 71 0.060
61
CRN025 Corneal Dystrophy 42 0.059
62
HYP022 Hypohidrosis 36 0.059
63
ADT003 Auditory System Disease 44 0.059
64
P ALP009 Alopecia Areata 64 0.055
65
VST004 Vestibular Disease 45 0.055
66
AMB002 Amblyopia 45 0.054
67
PLM017 Pulmonary Alveolar Microlithiasis 48 0.052
68
P ERY053 Erythrokeratodermia Variabilis Et Progressiva 1 51 0.051
69
c ALP061 Alopecia, Androgenetic, 1 44 0.051
70
MMB001 Membranoproliferative Glomerulonephritis 51 0.050
71
P ANX007 Anauxetic Dysplasia 1 36 0.046
72
ALP097 Alopecia Universalis Congenita 40 0.045
73
c CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 53 0.044
74
P EPL140 Epilepsy, Idiopathic Generalized 58 0.043
75
STR046 Stargardt Macular Degeneration 30 0.041
76
SWT003 Sweat Gland Disease 42 0.040
77
TLG001 Telogen Effluvium 30 0.040
78
P MGL001 Megaloblastic Anemia 52 0.039
79
CLF004 Cleft Lip/palate 49 0.037
80
c GRV008 Graves Disease 1 52 0.035
81
BRS056 Breast Metaplastic Carcinoma 38 0.032
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