Search results for "hypotrichosis, localized, autosomal recessive, 3"

The MalaCard for "hypotrichosis, localized, autosomal recessive, 3" has been retired.
Searching MalaCards for entries containing "hypotrichosis, localized, autosomal recessive, 3"

147 hits were found for 'hypotrichosis, localized, autosomal recessive, 3'

# Family MCID Name MIFTS Score
1
c HYP559 Hypotrichosis 8 30 3.755
2
P HYP087 Hypotrichosis 44 0.334
3
ALR002 Al-Raqad Syndrome 36 0.233
4
RTN023 Retinitis 49 0.224
5
P ADN016 Adenocarcinoma 69 0.189
6
P GST049 Gastrointestinal System Cancer 59 0.146
7
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.145
8
ALP008 Alopecia 56 0.144
9
P THY032 Thyroiditis 57 0.141
10
c BRN108 Branchiootic Syndrome 1 36 0.134
11
P CTR002 Cataract 57 0.133
12
P PRD008 Periodontitis 46 0.127
13
P SKN013 Skin Benign Neoplasm 38 0.121
14
c CLL013 Cell Type Cancer 46 0.118
15
SNS001 Sensorineural Hearing Loss 52 0.117
16
TTH006 Tooth Disease 52 0.116
17
c HRD010 Hereditary Spastic Paraplegia 66 0.115
18
SKN016 Skin Disease 69 0.114
19
P LVR013 Liver Disease 76 0.112
20
P NRV006 Nervous System Cancer 62 0.111
21
P INT063 Intellectual Disability 46 0.111
22
P AMY004 Amyloidosis 63 0.110
23
END035 Endocrine Gland Cancer 50 0.109
24
ECT006 Ectodermal Dysplasia 46 0.107
25
P CRD011 Cardiomyopathy 66 0.104
26
c HYP507 Hypotrichosis 1 30 0.103
27
RCT018 Rectal Neoplasm 53 0.103
28
P SML001 Small Cell Carcinoma 54 0.100
29
P CHR071 Charcot-Marie-Tooth Disease 66 0.099
30
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 32 0.098
31
AYM001 Ayme-Gripp Syndrome 40 0.097
32
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 42 0.096
33
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 57 0.096
34
c BSL007 Basal Cell Carcinoma 66 0.094
35
P LYM025 Lymphedema 60 0.093
36
DRM006 Dermatitis 58 0.091
37
P GLM007 Glomerulonephritis 56 0.090
38
P RTN016 Retinal Degeneration 50 0.088
39
P INF032 Infertility 61 0.088
40
GST040 Gastric Adenocarcinoma 57 0.085
41
c CLD010 Cold-Induced Sweating Syndrome 1 43 0.083
42
CNR002 Cone-Rod Dystrophy 65 0.083
43
P PMP005 Pemphigus Vulgaris 47 0.083
44
P CRV031 Cervical Adenocarcinoma 52 0.081
45
KRT009 Keratosis 50 0.080
46
PRP019 Peripheral Nervous System Disease 52 0.079
47
EYD002 Eye Disease 62 0.079
48
P LNG064 Lung Cancer Susceptibility 3 62 0.078
49
MCR013 Microphthalmia 57 0.077
50
P HRD018 Hair Disease 48 0.077
51
CLR109 Colorectal Adenocarcinoma 50 0.076
52
P BRC006 Brachydactyly 53 0.075
53
ADT003 Auditory System Disease 49 0.075
54
TRN018 Transitional Cell Carcinoma 56 0.074
55
GLB003 Globe Disease 34 0.072
56
ATP002 Atopy 62 0.071
57
P TRM003 Tremor 54 0.071
58
P HMC003 Hemochromatosis 71 0.070
59
P SYN001 Syndactyly 49 0.070
60
P PLY019 Polyneuropathy 53 0.070
61
ANH002 Anhidrosis 42 0.070
62
P SNS014 Sinusitis 66 0.069
63
P ESN007 Eosinophilia 61 0.066
64
P TRC086 Trichohepatoenteric Syndrome 1 46 0.065
65
P ATP001 Atopic Dermatitis 60 0.063
66
LKC003 Leukocyte Disease 45 0.062
67
MXD023 Mixed Cell Type Cancer 45 0.062
68
HYP022 Hypohidrosis 41 0.061
69
CNG008 Congenital Ichthyosiform Erythroderma 52 0.060
70
PPL002 Papillary Carcinoma 50 0.060
71
DRM014 Dermatofibrosarcoma Protuberans 61 0.059
72
STR046 Stargardt Macular Degeneration 27 0.059
73
P HLP001 Holoprosencephaly 62 0.058
74
CLF001 Cleft Lip 48 0.058
75
P PHC003 Pheochromocytoma 72 0.058
76
c MLG077 Malignant Peripheral Nerve Sheath Tumor 56 0.057
77
P ORG009 Organ System Cancer 45 0.057
78
ALP001 Alopecia Universalis 57 0.057
79
EYL005 Eyelid Disease 41 0.056
80
P LKM068 Leukemia, Chronic Myeloid, Somatic 65 0.056
81
P ALP009 Alopecia Areata 62 0.055
82
ADR016 Adrenal Cortical Carcinoma 60 0.054
83
MRK001 Merkel Cell Carcinoma 56 0.054
84
GST078 Gastrointestinal Allergy 41 0.054
85
P UVT001 Uveitis 60 0.054
86
c SML034 Small Cell Neuroendocrine Carcinoma 41 0.054
87
c STR084 Stargardt Disease 1 48 0.053
88
CRV026 Cervical Clear Cell Adenocarcinoma 34 0.053
89
CRB002 Cerebral Primitive Neuroectodermal Tumor 42 0.052
90
c LBR014 Leber Congenital Amaurosis 4 41 0.052
91
EWN002 Ewing's Family of Tumors 45 0.051
92
P PRM001 Primary Cutaneous Amyloidosis 54 0.051
93
c MCL042 Macular Degeneration, Age-Related, 1 71 0.051
94
P OCL013 Oculodentodigital Dysplasia 58 0.051
95
BSL006 Basaloid Squamous Cell Carcinoma 40 0.050
96
ACN001 Acinar Cell Carcinoma 48 0.050
97
ALL009 Allergic Conjunctivitis 51 0.050
98
c TRC092 Trichorhinophalangeal Syndrome, Type I 44 0.050
99
MCN001 Mucinous Adenocarcinoma 48 0.049
100
MMB001 Membranoproliferative Glomerulonephritis 44 0.049
101
P OLG002 Oligodendroglioma 55 0.048
102
MST016 Mesothelioma, Somatic 52 0.048
103
CNJ012 Conjunctival Disease 48 0.048
104
RBR001 Roberts Syndrome 61 0.047
105
NTH001 Netherton Syndrome 52 0.047
106
P DYS021 Dysautonomia 47 0.046
107
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 53 0.046
108
LVR002 Liver Angiosarcoma 44 0.046
109
MGL001 Megaloblastic Anemia 51 0.046
110
P MST009 Mastocytosis 54 0.046
111
c CLL012 Cell Type Benign Neoplasm 41 0.045
112
HDR006 Hidradenocarcinoma 42 0.045
113
P CYS017 Cystic Teratoma 40 0.045
114
CTN014 Cutaneous Mastocytosis 49 0.045
115
ODN006 Odontoma 34 0.045
116
c PRK031 Parkinson Disease 1 54 0.044
117
SPN032 Spindle Cell Carcinoma 44 0.044
118
PRG008 Paragonimiasis 40 0.044
119
P ESN008 Eosinophilic Pneumonia 47 0.044
120
DSM007 Desmoplastic Small Round Cell Tumor 49 0.043
121
URT008 Urticaria Pigmentosa 37 0.043
122
P BRS017 Breast Adenomyoepithelioma 27 0.042
123
BRS058 Breast Myoepithelial Neoplasm 23 0.042
124
BLR005 Biliary Papillomatosis 34 0.042
125
FDL002 Food Allergy 56 0.042
126
c GST048 Gastrointestinal System Benign Neoplasm 40 0.042
127
PLM035 Pulmonary Eosinophilia 46 0.042
128
P STH001 Saethre-Chotzen Syndrome 61 0.042
129
c SYS004 Systemic Mastocytosis 60 0.041
130
MNN008 Meningeal Melanomatosis 34 0.041
131
CHR001 Churg-Strauss Syndrome 48 0.041
132
INT004 Intraneural Perineurioma 33 0.040
133
SCR001 Secretory Meningioma 36 0.040
134
NSL003 Nasal Cavity Adenocarcinoma 40 0.039
135
c BLD008 Bladder Carcinoma in Situ 33 0.039
136
INT040 Intrinsic Asthma 40 0.039
137
ILM001 Ileum Cancer 35 0.039
138
NDL007 Nodular Goiter 44 0.039
139
BLD019 Bile Duct Cystadenocarcinoma 32 0.039
140
c MLG053 Malignant Ovarian Brenner Tumor 38 0.039
141
c INT282 Integumentary System Benign Neoplasm 21 0.039
142
c GRV008 Graves Disease 1 44 0.038
143
CRN273 Corneal Dystrophy, Subepithelial Mucinous 29 0.038
144
KMR001 Kimura Disease 50 0.037
145
PPL039 Papillary Glioneuronal Tumor 31 0.037
146
ACH005 Achalasia 55 0.037
147
BLS003 Blastoma 37 0.036