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"

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

# Family MCID Name MIFTS Score
1
c HYP559 Hypotrichosis 8 31 4.069
2
P HYP087 Hypotrichosis 45 0.317
3
RTN023 Retinitis 49 0.207
4
ALR002 Al-Raqad Syndrome 36 0.169
5
SKN016 Skin Disease 68 0.148
6
AND005 Androgen Insensitivity Syndrome, Mild 16 0.128
7
P THY032 Thyroiditis 54 0.127
8
P GST049 Gastrointestinal System Cancer 60 0.125
9
HPT074 Hepatic Adenoma, Somatic 51 0.125
10
HNM002 Hinman Syndrome 25 0.124
11
P CTR002 Cataract 57 0.122
12
ALP008 Alopecia 55 0.114
13
P PRD008 Periodontitis 46 0.113
14
SNS001 Sensorineural Hearing Loss 57 0.107
15
ADT003 Auditory System Disease 51 0.106
16
c BRN108 Branchiootic Syndrome 1 36 0.103
17
TTH006 Tooth Disease 52 0.101
18
ECT006 Ectodermal Dysplasia 47 0.098
19
c CLL013 Cell Type Cancer 48 0.097
20
c HYP507 Hypotrichosis 1 29 0.096
21
P AMY004 Amyloidosis 64 0.094
22
P CRD011 Cardiomyopathy 67 0.092
23
P INT063 Intellectual Disability 53 0.090
24
c HRD010 Hereditary Spastic Paraplegia 65 0.089
25
RCT018 Rectal Neoplasm 55 0.089
26
c BSL007 Basal Cell Carcinoma 64 0.087
27
DRM006 Dermatitis 61 0.086
28
P SML001 Small Cell Carcinoma 57 0.085
29
P LYM025 Lymphedema 61 0.084
30
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 55 0.084
31
P INF032 Infertility 61 0.083
32
P CHR071 Charcot-Marie-Tooth Disease 66 0.083
33
MST019 Mastoiditis 33 0.083
34
P RTN016 Retinal Degeneration 54 0.081
35
AYM001 Ayme-Gripp Syndrome 45 0.080
36
KRT009 Keratosis 50 0.077
37
P GLM007 Glomerulonephritis 56 0.076
38
EYD002 Eye Disease 63 0.074
39
P AST005 Asthma 82 0.073
40
P HRD018 Hair Disease 50 0.073
41
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 37 0.072
42
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 47 0.072
43
CNR002 Cone-Rod Dystrophy 68 0.071
44
GST040 Gastric Adenocarcinoma 52 0.071
45
P ATP001 Atopic Dermatitis 62 0.070
46
P PRP019 Peripheral Nervous System Disease 54 0.070
47
GLB003 Globe Disease 35 0.069
48
THY028 Thyroid Cancer 68 0.069
49
P CRV031 Cervical Adenocarcinoma 52 0.067
50
MCR013 Microphthalmia 59 0.066
51
P HYP069 Hyperparathyroidism 57 0.065
52
P BRC006 Brachydactyly 52 0.064
53
P STR020 Strabismus 53 0.064
54
CLR109 Colorectal Adenocarcinoma 50 0.063
55
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 58 0.063
56
ATP002 Atopy 63 0.061
57
P TRM003 Tremor 54 0.060
58
P LYM033 Lymphoproliferative Syndrome 53 0.058
59
ADP007 Adie Pupil 34 0.057
60
HYD057 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 44 0.057
61
EYL005 Eyelid Disease 42 0.056
62
P LNG064 Lung Cancer Susceptibility 3 62 0.056
63
BRN028 Brain Cancer 70 0.056
64
P TRC086 Trichohepatoenteric Syndrome 1 46 0.055
65
P PLY019 Polyneuropathy 54 0.055
66
ANH002 Anhidrosis 42 0.054
67
P HMC003 Hemochromatosis 72 0.054
68
CRN025 Corneal Dystrophy 41 0.054
69
LKC003 Leukocyte Disease 47 0.053
70
RBR001 Roberts Syndrome 59 0.053
71
P ESN007 Eosinophilia 61 0.053
72
CLF001 Cleft Lip 49 0.052
73
MXD023 Mixed Cell Type Cancer 47 0.052
74
P HLP001 Holoprosencephaly 62 0.051
75
HYP022 Hypohidrosis 42 0.050
76
P ALP009 Alopecia Areata 61 0.050
77
PPL002 Papillary Carcinoma 49 0.050
78
NRP015 Neuropathy, Congenital Hypomyelinating 56 0.048
79
CNG008 Congenital Ichthyosiform Erythroderma 53 0.048
80
URB001 Urbach-Wiethe Disease 48 0.048
81
DRM014 Dermatofibrosarcoma Protuberans 60 0.047
82
SPL040 Split Hand 37 0.046
83
GST078 Gastrointestinal Allergy 41 0.046
84
P LKM068 Leukemia, Chronic Myeloid, Somatic 66 0.045
85
NTH001 Netherton Syndrome 52 0.044
86
P EPN002 Ependymoma 53 0.044
87
c LRG001 Large Cell Carcinoma 51 0.043
88
STR046 Stargardt Macular Degeneration 29 0.043
89
ALP001 Alopecia Universalis 57 0.043
90
c TRC092 Trichorhinophalangeal Syndrome, Type I 45 0.042
91
CNJ012 Conjunctival Disease 46 0.041
92
c SML034 Small Cell Neuroendocrine Carcinoma 40 0.041
93
P UVT001 Uveitis 59 0.041
94
FDL002 Food Allergy 54 0.041
95
ALL009 Allergic Conjunctivitis 51 0.041
96
P OCL013 Oculodentodigital Dysplasia 59 0.041
97
MRK001 Merkel Cell Carcinoma 51 0.041
98
c ESS001 Essential Tremor 61 0.040
99
MCN001 Mucinous Adenocarcinoma 50 0.040
100
P OLG002 Oligodendroglioma 55 0.040
101
PNN001 Panniculitis 50 0.039
102
CRB002 Cerebral Primitive Neuroectodermal Tumor 45 0.039
103
SPL039 Split Foot 33 0.039
104
P HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 58 0.039
105
P DYS021 Dysautonomia 47 0.039
106
c PRK031 Parkinson Disease 1 55 0.039
107
MMB001 Membranoproliferative Glomerulonephritis 45 0.039
108
CRV026 Cervical Clear Cell Adenocarcinoma 36 0.039
109
AML029 Ameloblastoma 46 0.038
110
EWN002 Ewing's Family of Tumors 45 0.038
111
c LBR014 Leber Congenital Amaurosis 4 47 0.037
112
ADR016 Adrenal Cortical Carcinoma 61 0.037
113
CRB027 Cerebellar Disease 47 0.037
114
DDN010 Duodenum Cancer 44 0.036
115
BSL006 Basaloid Squamous Cell Carcinoma 41 0.036
116
P MST009 Mastocytosis 54 0.035
117
OPT008 Optic Nerve Neoplasm 40 0.035
118
c STR084 Stargardt Disease 1 52 0.035
119
DSM007 Desmoplastic Small Round Cell Tumor 47 0.034
120
MST016 Mesothelioma, Somatic 53 0.034
121
P STH001 Saethre-Chotzen Syndrome 59 0.034
122
INT040 Intrinsic Asthma 40 0.034
123
PRG008 Paragonimiasis 39 0.034
124
c GRV008 Graves Disease 1 45 0.033
125
P CYS017 Cystic Teratoma 41 0.033
126
P DSB006 Desbuquois Dysplasia 1 53 0.033
127
ACH005 Achalasia 54 0.033
128
CTN014 Cutaneous Mastocytosis 48 0.032
129
SRC002 Sarcomatoid Renal Cell Carcinoma 41 0.032
130
c GST048 Gastrointestinal System Benign Neoplasm 41 0.032
131
URT008 Urticaria Pigmentosa 38 0.032
132
c ANT034 Anterior Uveitis 49 0.032
133
CRN273 Corneal Dystrophy, Subepithelial Mucinous 28 0.032
134
ODN006 Odontoma 34 0.032
135
c PRK059 Parkinson Disease 8 52 0.031
136
PLM035 Pulmonary Eosinophilia 46 0.031
137
KMR001 Kimura Disease 48 0.031
138
BLS003 Blastoma 37 0.031
139
LVR002 Liver Angiosarcoma 44 0.031
140
c SYS004 Systemic Mastocytosis 59 0.030
141
CHR001 Churg-Strauss Syndrome 49 0.030
142
HDR006 Hidradenocarcinoma 42 0.030
143
ESN005 Eosinophilic Gastroenteritis 49 0.030
144
GNT002 Giant Cell Glioblastoma 51 0.030
145
c LNG031 Lung Benign Neoplasm 44 0.030
146
P ESN008 Eosinophilic Pneumonia 49 0.030
147
c PRK025 Parkinson Disease 10 42 0.030
148
LTX001 Latex Allergy 38 0.030
149
CLF027 Cleft Palate, Isolated 56 0.029
150
SWT002 Sweat Gland Cancer 40 0.029
151
BLR005 Biliary Papillomatosis 33 0.029
152
P BRS017 Breast Adenomyoepithelioma 28 0.029
153
BRS058 Breast Myoepithelial Neoplasm 23 0.029
154
c INT282 Integumentary System Benign Neoplasm 20 0.029
155
INT004 Intraneural Perineurioma 33 0.029
156
SCR001 Secretory Meningioma 41 0.028
157
NSL003 Nasal Cavity Adenocarcinoma 40 0.028
158
c BLD008 Bladder Carcinoma in Situ 35 0.028
159
STT002 Status Asthmaticus 43 0.027
160
CRB028 Cerebellar Medulloblastoma 34 0.027
161
BLD019 Bile Duct Cystadenocarcinoma 32 0.027
162
OPT007 Optic Nerve Glioma 43 0.027
163
c MLG053 Malignant Ovarian Brenner Tumor 40 0.027
164
PNC019 Pancreatoblastoma 32 0.027
165
PPL039 Papillary Glioneuronal Tumor 30 0.027