The MalaCard for "hypodontia" has been retired.
Searching MalaCards for entries containing "hypodontia"

212 hits were found for 'hypodontia'

# ++ Fam MCID Name MIFTS Score
1
MCR072 Microdontia Hypodontia Short Stature 1 3.993
2
PLR009 Pol Iii-Related Leukodystrophies 42 3.974
3
HYP196 Hypodontia, X-Linked 1 3.954
4
SCH038 Schopf-Schulz-Passarge Syndrome 20 3.447
5
c EPD051 Epidermolysis Bullosa Simplex with Anodontia/hypodontia 11 3.447
6
TTH003 Tooth and Nail Syndrome 22 2.847
7
ECT063 Ectodermal Dysplasia 3, Witkop Type 15 2.823
8
CNG098 Congenital Heart Disease Ptosis Hypodontia Craniostosis 1 2.823
9
HYP195 Hypodontia of Incisors and Premolars 0 2.796
10
TTH002 Tooth Agenesis 38 2.104
11
ADL002 Adult Syndrome 50 2.041
12
DFN015 Deafness Oligodontia Syndrome 11 2.013
13
c AXN002 Axenfeld-Rieger Syndrome 57 1.977
14
MHT001 Mehta Lewis Patton Syndrome 2 1.977
15
ZDK001 Zadik Barak Levin Syndrome 1 1.977
16
P TTH016 Tooth Agenesis, Selective, 1, with or Without Orofacial Cleft 34 0.175
17
P MYP018 Myopia 6 23 0.152
18
P ECT006 Ectodermal Dysplasia 46 0.138
19
c HYP087 Hypotrichosis 41 0.107
20
P HYP013 Hypohidrotic Ectodermal Dysplasia 57 0.098
21
P AML002 Amelogenesis Imperfecta 47 0.088
22
AND001 Anodontia 44 0.088
23
TRD003 Taurodontism 29 0.088
24
P CLF002 Cleft Palate 60 0.076
25
NSY001 N Syndrome 57 0.076
26
HYP080 Hypogonadism 54 0.076
27
c EPD016 Epidermolysis Bullosa 53 0.076
28
ECT061 Ectodermal Dysplasia 10a, Hypohidrotic/hair/nail Type, Autosomal Dominant 33 0.076
29
PSY004 Psychotic Disorder 62 0.062
30
P STR020 Strabismus 53 0.062
31
P STS001 Sotos Syndrome 46 0.062
32
OTP004 Oto-Palato-Digital Syndrome Type 1 34 0.062
33
P ATS061 Autosomal Recessive Hypotrichosis 32 0.062
34
BRD005 Borderline Leprosy 32 0.062
35
WYR002 Weyers Acrofacial Dysostosis 26 0.062
36
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 24 0.062
37
BLM001 Bloom Syndrome 74 0.044
38
P SMT004 Smith-Lemli-Opitz Syndrome 72 0.044
39
P ALG002 Alagille Syndrome 68 0.044
40
PRG004 Progeria 68 0.044
41
CLD001 Cleidocranial Dysplasia 68 0.044
42
LRN002 Laron Syndrome 65 0.044
43
P CNG026 Congenital Heart Defect 65 0.044
44
P SHR002 Short Stature 64 0.044
45
P RTH001 Rothmund-Thomson Syndrome 63 0.044
46
c CRN037 Craniosynostosis 62 0.044
47
OCL005 Oculocerebrorenal Syndrome 61 0.044
48
CFF002 Coffin-Lowry Syndrome 60 0.044
49
WLF001 Wolff-Parkinson-White Syndrome 60 0.044
50
P EPD003 Epidermolysis Bullosa Simplex 59 0.044
51
ALP008 Alopecia 59 0.044
52
CHR003 Cherubism 58 0.044
53
SMT015 Smith Magenis Syndrome 58 0.044
54
CLB001 Coloboma 56 0.044
55
FCL009 Focal Dermal Hypoplasia 56 0.044
56
P SHR029 Short Syndrome 55 0.044
57
SNS001 Sensorineural Hearing Loss 55 0.044
58
LDD001 Ladd Syndrome 54 0.044
59
LRN003 Learning Disability 54 0.044
60
P LKD001 Leukodystrophy 53 0.044
61
P FNC004 Fanconi Syndrome 52 0.044
62
c SYN001 Syndactyly 52 0.044
63
WLF002 Wolf-Hirschhorn Syndrome 51 0.044
64
P WVR001 Weaver Syndrome 51 0.044
65
c MNT147 Mental Retardation 51 0.044
66
ANK001 Ankylosis 51 0.044
67
SNG010 Single Median Maxillary Central Incisor 50 0.044
68
KRT009 Keratosis 49 0.044
69
c CTR002 Cataract 48 0.044
70
P DNT009 Dentin Dysplasia 46 0.044
71
WLL001 Williams-Beuren Syndrome 46 0.044
72
P FRS003 Fraser Syndrome 46 0.044
73
JHN001 Johanson-Blizzard Syndrome 45 0.044
74
ULN003 Ulnar-Mammary Syndrome 45 0.044
75
BRS002 Beare-Stevenson Cutis Gyrata Syndrome 45 0.044
76
c TYP003 Type I Ehlers-Danlos Syndrome 45 0.044
77
P MBS002 Moebius Syndrome 45 0.044
78
CHN016 Cohen Syndrome 44 0.044
79
P OCL013 Oculodentodigital Dysplasia 44 0.044
80
BRN003 Branchiooculofacial Syndrome 44 0.044
81
ELL001 Ellis-Van Creveld Syndrome 44 0.044
82
KRT012 Keratoderma 44 0.044
83
BLC003 Bloch-Sulzberger Syndrome 44 0.044
84
P CHN005 Choanal Atresia 43 0.044
85
OST044 Osteoglophonic Dysplasia 42 0.044
86
CHR101 Char Syndrome 42 0.044
87
RTR008 Root Resorption 41 0.044
88
P STC005 Stickler Syndrome Type 1 41 0.044
89
P HYP514 Hypogonadotropic Hypogonadism 8 with or Without Anosmia 41 0.044
90
PPL006 Papillon-Lefevre Disease 41 0.044
91
SCH016 Schimke Immunoosseous Dysplasia 40 0.044
92
HYP022 Hypohidrosis 40 0.044
93
P AXN003 Axenfeld-Rieger Syndrome Type 1 39 0.044
94
P PRR010 Pierre Robin Sequence 39 0.044
95
HYP030 Hypoactive Sexual Desire Disorder 39 0.044
96
FGS001 Fg Syndrome 39 0.044
97
PRT093 Proteus Syndrome, Somatic 39 0.044
98
RPP001 Rapp-Hodgkin Syndrome 37 0.044
99
MLN014 Melnick-Needles Syndrome 37 0.044
100
c MYP006 Myopia 36 0.044
101
TTR016 Tetra-Amelia Syndrome 36 0.044
102
P TRC071 Treacher Collins Syndrome 3 35 0.044
103
OCL014 Oculofaciocardiodental Syndrome 35 0.044
104
P CRN139 Cornelia De Lange Syndrome 1 34 0.044
105
OTP005 Oto-Palato-Digital Syndrome Type 2 34 0.044
106
P RBN011 Robinow Syndrome, Autosomal Dominant 34 0.044
107
VND002 Van Der Woude Syndrome 34 0.044
108
P SPL040 Split Hand 33 0.044
109
c SPL037 Split Hand Foot Malformation 33 0.044
110
PLT008 Pili Torti 32 0.044
111
c SPL039 Split Foot 32 0.044
112
ACT164 Actinic Prurigo 32 0.044
113
TTH001 Tooth Ankylosis 31 0.044
114
P CRN108 Cranioectodermal Dysplasia 1 31 0.044
115
P MCR044 Microcephalic Osteodysplastic Primordial Dwarfism Type 2 30 0.044
116
OLM001 Olmsted Syndrome 30 0.044
117
c RBN009 Robinow Syndrome, Autosomal Recessive 29 0.044
118
ORL010 Oral-Facial-Digital Syndrome Type I 29 0.044
119
12Q002 12q14 Microdeletion Syndrome 28 0.044
120
HNN001 Hennekam Syndrome 28 0.044
121
FGF001 Fgfr-Related Craniosynostosis Syndromes 28 0.044
122
P SCK023 Seckel Syndrome Type 1 27 0.044
123
P KBK002 Kabuki Syndrome 1 27 0.044
124
ODN006 Odontoma 26 0.044
125
2Q3003 2q32q33 Microdeletion Syndrome 25 0.044
126
SBS006 Sebastian Syndrome 25 0.044
127
P OPT051 Opitz Gbbb Syndrome, Type I 25 0.044
128
P KLN006 Koolen-De Vries Syndrome 25 0.044
129
KBG001 Kbg Syndrome 25 0.044
130
c ATS004 Autosomal Dominant Microcephaly 25 0.044
131
ECT071 Ectodermal Dysplasia 1, Hypohidrotic, X-Linked 24 0.044
132
YNS001 Yunis Varon Syndrome 24 0.044
133
ZNC001 Zunich Neuroectodermal Syndrome 23 0.044
134
P VRT007 Vertical Talus, Congenital 23 0.044
135
ZLT002 Zlotogora Syndrome 22 0.044
136
ECT042 Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/palate Syndrome 3 22 0.044
137
DFN017 Deafness Onychodystrophy Osteodystrophy and Mental Retardation Syndrome 22 0.044
138
P CNG044 Congenital Deafness with Labyrinthine Aplasia, Microtia, and Microdontia 22 0.044
139
CLF027 Cleft Palate, Isolated 21 0.044
140
ANK009 Ankyloblepharon-Ectodermal Defects-Cleft Lip/palate Syndrome 21 0.044
141
RCH006 Richieri Costa Pereira Syndrome 21 0.044
142
SYN016 Syndactyly Cenani Lenz Type 21 0.044
143
HYP465 Hypoglossia - Hypodactyly 21 0.044
144
P OTD002 Otodental Syndrome 21 0.044
145
c HYP253 Hypohidrotic Ectodermal Dysplasia, Autosomal 20 0.044
146
c ORF007 Orofaciodigital Syndrome 2 20 0.044
147
ODN009 Odontoonychodermal Dysplasia 20 0.044
148
P 19P001 19p13.12 Microdeletion Syndrome 19 0.044
149
GRL002 Gorlin Chaudhry Moss Syndrome 19 0.044
150
ACR029 Acrofacial Dysostosis Catania Type 19 0.044
151
EMS001 Eem Syndrome 18 0.044
152
MNT038 Mental Retardation, Epileptic Seizures, Hypogonadism and Hypogenitalism, Microcephaly, and Obesity 17 0.044
153
ODN015 Odontotrichomelic Syndrome 17 0.044
154
TRC048 Trichodental Syndrome 17 0.044
155
MXL012 Maxillo-Nasal Dysplasia 16 0.044
156
PRG079 Progeria - Short Stature - Pigmented Nevi 16 0.044
157
AML005 Amelogenesis Imperfecta Hypomaturation Type 16 0.044
158
CRB135 Cerebro-Oculo-Nasal Syndrome 15 0.044
159
LWR007 Lowry Maclean Syndrome 15 0.044
160
AML038 Amelogenesis Imperfecta and Gingival Fibromatosis Syndrome 15 0.044
161
CRN190 Craniosynostosis - Fibular Aplasia 15 0.044
162
ICH026 Ichthyosis, Leukocyte Vacuoles, Alopecia, and Sclerosing Cholangitis 14 0.044
163
TBS002 Teebi Shaltout Syndrome 14 0.044
164
WLS004 Wilson-Turner Syndrome 14 0.044
165
ACR030 Acrofacial Dysostosis Palagonia Type 14 0.044
166
DRM023 Dermoodontodysplasia 14 0.044
167
PLL004 Pallister W Syndrome 14 0.044
168
ATS134 Autosomal Dominant Nail Dysplasia 14 0.044
169
BKS002 Book Syndrome 14 0.044
170
SHR027 Short Stature Wormian Bones Dextrocardia 13 0.044
171
CRN049 Craniolenticulosutural Dysplasia 13 0.044
172
DRM020 Dermatoosteolysis Kirghizian Type 13 0.044
173
OCL058 Oculodental Syndrome, Rutherfurd Type 13 0.044
174
CRN082 Craniofacial Dysostosis with Diaphyseal Hyperplasia 13 0.044
175
c DST072 Distal Monosomy 6p 13 0.044
176
FCC002 Faciocardiorenal Syndrome 12 0.044
177
CRB056 Cerebellar Ataxia Ectodermal Dysplasia 12 0.044
178
LLS001 Lelis Syndrome 12 0.044
179
PRG024 Progeroid Syndrome Petty Type 12 0.044
180
ACR077 Acro-Oto-Ocular Syndrome 12 0.044
181
STR034 Stratton-Garcia-Young Syndrome 11 0.044
182
TRC047 Tricho Retino Dento Digital Syndrome 11 0.044
183
SPL038 Splenogonadal Fusion - Limb Defects - Micrognathia 11 0.044
184
BLP009 Blepharonasofacial Malformation Syndrome 11 0.044
185
CRN223 Craniofaciofrontodigital Syndrome 11 0.044
186
NNR006 Non-Eruption of Teeth - Maxillary Hypoplasia - Genu Valgum 10 0.044
187
ECT015 Ectodermal Dysplasia Berlin Type 10 0.044
188
PLD002 Pilodental Dysplasia with Refractive Errors 10 0.044
189
AML012 Ameloonychohypohidrotic Syndrome 10 0.044
190
CNG240 Congenital Unilateral Hypoplasia of Depressor Anguli Oris 10 0.044
191
TRD002 Taurodontia Absent Teeth Sparse Hair 10 0.044
192
EXT038 Extrasystoles Short Stature Hyperpigmentation Microcephaly 9 0.044
193
OCL056 Oculoosteocutaneous Syndrome 9 0.044
194
ANK005 Ankyloblepharon Filiforme Imperforate Anus 9 0.044
195
PLY032 Polydactyly Postaxial Dental and Vertebral 9 0.044
196
ECT021 Ectodermal Dysplasia Trichoodontoonychial Type 9 0.044
197
TRC057 Trichoodontoonychial Dysplasia 9 0.044
198
MCR174 Macrocephaly - Short Stature - Paraplegia 8 0.044
199
PNH003 Pinheiro Freire-Maia Miranda Syndrome 8 0.044
200
ARR032 Arrhinia - Choanal Atresia - Microphthalmia 8 0.044
201
STL004 Stoll Alembik Finck Syndrome 7 0.044
202
CLF020 Cleft Palate Stapes Fixation Oligodontia 7 0.044
203
c HYP206 Hypohidrotic Ectodermal Dysplasia Autosomal Recessive 7 0.044
204
CRT029 Cortada Koussef Matsumoto Syndrome 7 0.044
205
INT225 Intellectual Deficit - Athetosis - Microphthalmia 7 0.044
206
SYM015 Symptomatic Form of Coffin-Lowry Syndrome in Female Carriers 6 0.044
207
CHR159 Charlie M Syndrome 6 0.044
208
CLF030 Cleft Lip/palate - Deafness - Sacral Lipoma 6 0.044
209
HRD049 Hereditary Koilonychia 6 0.044
210
ODN004 Odonto Onycho Dysplasia with Alopecia 6 0.044
211
c ECT058 Ectodermal Dysplasia 11b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 5 0.044
212
ECT060 Ectodermal Dysplasia 11a, Hypohidrotic/hair/tooth Type 5 0.044