Search results for "dental enamel hypoplasia"

The MalaCard for "dental enamel hypoplasia" has been retired.
Searching MalaCards for entries containing "dental enamel hypoplasia"

177 hits were found for 'dental enamel hypoplasia'

# Family MCID Name MIFTS Score
1
TRC050 Tricho-Dento-Osseous Syndrome 1 4 2.467
2
DNT001 Dental Fluorosis 43 0.342
3
ENM001 Enamel Caries 30 0.326
4
P AML002 Amelogenesis Imperfecta 43 0.216
5
GNG013 Gingivitis 60 0.207
6
FCL009 Focal Dermal Hypoplasia 54 0.197
7
P PRD008 Periodontitis 46 0.186
8
MTH009 Mouth Disease 63 0.157
9
AYM001 Ayme-Gripp Syndrome 45 0.132
10
c AML016 Amelogenesis Imperfecta, Type 1e 24 0.121
11
DFN007 Deafness Enamel Hypoplasia Nail Defects 23 0.115
12
c PND001 Pain Disorder 55 0.113
13
ECT006 Ectodermal Dysplasia 47 0.104
14
EPD016 Epidermolysis Bullosa 57 0.102
15
ALN003 Alaninuria with Microcephaly, Dwarfism, Enamel Hypoplasia, and Diabetes Mellitus 12 0.100
16
CDS002 Codas Syndrome 40 0.099
17
CLF001 Cleft Lip 49 0.097
18
P CLD001 Cleidocranial Dysplasia 62 0.096
19
BNS002 Bone Structure Disease 36 0.096
20
TRD003 Taurodontism 27 0.095
21
P HML047 Heimler Syndrome 1 18 0.095
22
P MCR010 Microcephaly 58 0.093
23
SMT004 Smith-Lemli-Opitz Syndrome 67 0.092
24
P RCK004 Rickets 59 0.092
25
CRB009 Cerebritis 38 0.089
26
ODN006 Odontoma 34 0.087
27
P OCL013 Oculodentodigital Dysplasia 59 0.086
28
WLL001 Williams-Beuren Syndrome 61 0.084
29
c AML050 Amelogenesis Imperfecta, Type if 18 0.082
30
STR032 Steroid Dehydrogenase Deficiency Dental Anomalies 11 0.080
31
PLY134 Polydactyly, Postaxial, with Dental and Vertebral Anomalies 15 0.080
32
LDD001 Ladd Syndrome 60 0.079
33
P INF032 Infertility 61 0.079
34
P TRC072 Treacher Collins Syndrome 1 52 0.078
35
P OST005 Osteogenesis Imperfecta 67 0.077
36
P EPL164 Epilepsy 66 0.077
37
P SCK009 Seckel Syndrome 1 46 0.076
38
P USH001 Usher Syndrome 52 0.076
39
SHH004 Shaheen Syndrome 25 0.075
40
P CTR002 Cataract 57 0.074
41
DWR001 Dwarfism 46 0.074
42
P PRD006 Prader-Willi Syndrome 63 0.073
43
P RBN001 Rubinstein-Taybi Syndrome 65 0.073
44
DRM006 Dermatitis 61 0.073
45
INC021 Incontinentia Pigmenti 60 0.073
46
P ATX004 Ataxia 53 0.071
47
P CND004 Candidiasis 57 0.071
48
c AML048 Amelogenesis Imperfecta, Type Ih 18 0.070
49
LWS003 Lowe Syndrome 61 0.070
50
KHL003 Kohlschutter-Tonz Syndrome 37 0.070
51
P TRN020 Turner Syndrome 64 0.069
52
49X002 49,xxxxy Syndrome 24 0.068
53
TTH002 Tooth Agenesis 55 0.068
54
RPP001 Rapp-Hodgkin Syndrome 48 0.067
55
CHR581 Chromosome 17q11.2 Deletion Syndrome, 1.4-Mb 32 0.067
56
P VLC001 Velocardiofacial Syndrome 62 0.067
57
CHR103 Charge Syndrome 64 0.067
58
ALL026 Allergic Hypersensitivity Disease 53 0.067
59
EPD062 Epidermolysis Bullosa, Junctional, Non-Herlitz Type 41 0.066
60
P HYP265 Hypotonia 39 0.066
61
ECT090 Ectodermal Dysplasia, Hypohidrotic, with Hypothyroidism and Agenesis of the Corpus Callosum 14 0.065
62
TBR024 Tuberous Sclerosis-1 65 0.065
63
ICH026 Ichthyosis, Leukocyte Vacuoles, Alopecia, and Sclerosing Cholangitis 25 0.065
64
MCR308 Microcephalic Primordial Dwarfism, Toriello Type 17 0.065
65
HLL013 Hall-Riggs Mental Retardation Syndrome 16 0.065
66
c PLT022 Pili Torti, Early-Onset 18 0.065
67
TRC029 Trichodontoosseous Syndrome 25 0.064
68
GST092 Gastroesophageal Reflux 61 0.063
69
P CLC005 Celiac Disease 67 0.062
70
c ORF037 Orofaciodigital Syndrome I 46 0.062
71
48X002 48,xxxy Syndrome 14 0.062
72
c MCP004 Mucopolysaccharidosis Iv 59 0.062
73
ALP091 Alopecia-Contractures-Dwarfism Mental Retardation Syndrome 19 0.062
74
PFF010 Pfeiffer-Palm-Teller Syndrome 13 0.062
75
HYP134 Hypoparathyroidism-Retardation-Dysmorphism Syndrome 41 0.061
76
NPH003 Nephrocalcinosis 46 0.061
77
P STC001 Stickler Syndrome 54 0.061
78
c USH003 Usher Syndrome Type Ii 42 0.061
79
APL002 Aplasia of Lacrimal and Salivary Glands 44 0.060
80
SCR025 Scarf Syndrome 18 0.059
81
HYP077 Hypertrichosis 52 0.058
82
48X003 48,xxyy Syndrome 25 0.058
83
PCK002 Pick Disease 67 0.058
84
P EXN002 Exanthem 57 0.058
85
P DRM007 Dermatitis Herpetiformis 46 0.058
86
CHN016 Cohen Syndrome 55 0.057
87
ARD001 Aredyld 20 0.057
88
OTD001 Otodental Dysplasia 25 0.056
89
c MCR261 Microphthalmia, Syndromic 2 33 0.056
90
DYS045 Dysosteosclerosis 22 0.055
91
c USH006 Usher Syndrome, Type 1b 51 0.055
92
KND001 Kindler Syndrome 50 0.055
93
P CRN108 Cranioectodermal Dysplasia 1 47 0.055
94
EPD050 Epidermolysis Bullosa Simplex with Muscular Dystrophy 37 0.055
95
EPD045 Epidermolysis Bullosa, Junctional, with Pyloric Stenosis 37 0.055
96
P KLN006 Koolen-De Vries Syndrome 37 0.055
97
EPD061 Epidermolysis Bullosa, Junctional, Herlitz Type 36 0.055
98
HYD052 Hydrocephalus, Sprengel Anomaly, and Costovertebral Dysplasia 15 0.055
99
TRC113 Trichoodontoonychial Dysplasia with Bone Deficiency 13 0.055
100
P SHR029 Short Syndrome 60 0.055
101
ACR002 Acrocapitofemoral Dysplasia 36 0.055
102
P PNC044 Pancreatitis 60 0.055
103
TTH005 Teeth Hard Tissue Disease 28 0.055
104
DNT045 Dental Anomalies and Short Stature 23 0.055
105
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 39 0.055
106
CTS003 Coats Disease 57 0.054
107
BND014 Bone Development Disease 42 0.053
108
ATP002 Atopy 63 0.053
109
P OST001 Osteopetrosis 62 0.053
110
CNN011 Cenani-Lenz Syndactyly Syndrome 31 0.052
111
CHR063 Chronic Mucocutaneous Candidiasis 61 0.052
112
P SJG002 Sjogren-Larsson Syndrome 51 0.052
113
ART037 Arthrogryposis and Ectodermal Dysplasia 19 0.052
114
DFN309 Deafness, Conductive, with Ptosis and Skeletal Anomalies 15 0.052
115
OST146 Osteopenia-Myopia-Hearing Loss-Intellectual Disability-Facial Dysmorphism Syndrome 9 0.052
116
SNS001 Sensorineural Hearing Loss 57 0.052
117
c OCL047 Oculodentodigital Dysplasia, Autosomal Recessive 21 0.052
118
SPN060 Spondylocarpotarsal Synostosis Syndrome 35 0.051
119
RNS001 Raine Syndrome 39 0.050
120
CRD119 Cardiac Arrest 63 0.049
121
LNZ003 Lenz-Majewski Hyperostotic Dwarfism 29 0.049
122
P MCR129 Microvascular Complications of Diabetes 1 57 0.049
123
c BRN108 Branchiootic Syndrome 1 36 0.048
124
HYW001 Hay-Wells Syndrome 33 0.048
125
OHD004 Ohdo Syndrome 32 0.048
126
c HML046 Heimler Syndrome 2 15 0.048
127
P STR020 Strabismus 53 0.048
128
P HYP087 Hypotrichosis 45 0.046
129
c LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 38 0.046
130
P MCR258 Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii 34 0.046
131
VSC007 Vascular Disease 67 0.046
132
P EPD009 Epidermolysis Bullosa Dystrophica 54 0.046
133
c MCP038 Mucopolysaccharidosis Iva 49 0.046
134
KBG001 Kbg Syndrome 49 0.046
135
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 31 0.046
136
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 47 0.046
137
CLF037 Cleft Lip/palate-Ectodermal Dysplasia Syndrome 27 0.046
138
BSL036 Basal Cell Nevus Syndrome 65 0.044
139
P CMR001 Camurati-Engelmann Disease 59 0.044
140
P AND016 Andersen Syndrome 58 0.044
141
PTT037 Pituitary Tumors 45 0.044
142
PHC004 Phace Syndrome 21 0.044
143
c PSD067 Pseudohypoparathyroidism Ia 52 0.043
144
ATM033 Autoimmune Polyendocrinopathy Syndrome , Type I, with or Without Reversible Metaphyseal Dysplasia 51 0.043
145
PRD003 Periodontosis 41 0.043
146
P VTM008 Vitamin D-Dependent Rickets, Type I 36 0.043
147
KRT014 Keratosis Follicularis Spinulosa Decalvans 26 0.043
148
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 22 0.043
149
RTN017 Retinal Detachment 57 0.042
150
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 31 0.042
151
EPD052 Epidermolysis Bullosa Simplex Superficialis 20 0.042
152
CRN082 Craniofacial Dysostosis with Diaphyseal Hyperplasia 16 0.042
153
CMB055 Combined Immunodeficiency Due to Crac Channel Dysfunction 11 0.042
154
GLC006 Galactosemia 67 0.039
155
ART005 Arteriovenous Malformation 65 0.039
156
P RFS001 Refsum Disease 62 0.039
157
PMS001 Poems Syndrome 55 0.039
158
P EPD003 Epidermolysis Bullosa Simplex 51 0.039
159
PSD014 Pseudopseudohypoparathyroidism 50 0.039
160
PRC012 Pericardial Effusion 50 0.039
161
LMB062 Limb Ischemia 48 0.039
162
DBT006 Diabetic Macular Edema 47 0.039
163
P TMR011 Tumoral Calcinosis, Hyperphosphatemic, Familial 46 0.039
164
HYD057 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 44 0.039
165
RCK007 Rickets, Vitamin D-Resistant, Type Iia 37 0.039
166
c EPD044 Epidermolysis Bullosa Dystrophica, Ar 36 0.039
167
STV004 Stuve-Wiedemann Syndrome/schwartz-Jampel Type 2 Syndrome 32 0.039
168
c EPD058 Epidermolysis Bullosa Simplex, Recessive 1 29 0.039
169
c MCP023 Mucopolysaccharidosis Type Ivb 27 0.039
170
c PSD058 Pseudohypoparathyroidism Ic 25 0.039
171
HMM004 Hamamy Syndrome 23 0.039
172
ECT073 Ectodermal Dysplasia/short Stature Syndrome 20 0.039
173
XFP001 Xfe Progeroid Syndrome 19 0.039
174
LCH010 Lichtenstein Syndrome 17 0.039
175
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 16 0.039
176
THR039 Thrombocytopenia Robin Sequence 13 0.039
177
48X005 48,xyyy 13 0.039