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

195 hits were found for 'hypodontia'

# Family MCID Name MIFTS Score
1
MCR072 Microdontia Hypodontia Short Stature 2 3.997
2
PLR009 Pol Iii-Related Leukodystrophies 56 3.977
3
HYP196 Hypodontia, X-Linked 1 3.956
4
SCH038 Schopf-Schulz-Passarge Syndrome 28 3.450
5
EPD051 Epidermolysis Bullosa Simplex with Anodontia/hypodontia 16 3.450
6
TTH003 Tooth and Nail Syndrome 28 2.871
7
ECT063 Ectodermal Dysplasia 3, Witkop Type 22 2.826
8
CNG098 Congenital Heart Disease Ptosis Hypodontia Craniostosis 1 2.826
9
HYP195 Hypodontia of Incisors and Premolars 0 2.797
10
TTH002 Tooth Agenesis 40 2.109
11
ADL002 Adult Syndrome 52 2.044
12
DFN015 Deafness Oligodontia Syndrome 14 2.015
13
c AXN002 Axenfeld-Rieger Syndrome 60 1.978
14
MHT001 Mehta Lewis Patton Syndrome 2 1.978
15
ZDK001 Zadik Barak Levin Syndrome 1 1.978
16
TTH016 Tooth Agenesis, Selective, 1, with or Without Orofacial Cleft 37 0.180
17
P MYP018 Myopia 6 29 0.156
18
c HYP087 Hypotrichosis 43 0.110
19
HYP013 Hypohidrotic Ectodermal Dysplasia 58 0.101
20
AND001 Anodontia 48 0.090
21
c AML002 Amelogenesis Imperfecta 47 0.090
22
P HYP080 Hypogonadism 60 0.078
23
P CLF002 Cleft Palate 59 0.078
24
HYP064 Hypogonadotropism 48 0.078
25
ECT061 Ectodermal Dysplasia 10a, Hypohidrotic/hair/nail Type, Autosomal Dominant 42 0.078
26
PSY004 Psychotic Disorder 69 0.064
27
DWN001 Down Syndrome 62 0.064
28
EPD016 Epidermolysis Bullosa 59 0.064
29
CLF001 Cleft Lip 59 0.064
30
P STR020 Strabismus 56 0.064
31
c STS001 Sotos Syndrome 45 0.064
32
OTP004 Oto-Palato-Digital Syndrome Type 1 44 0.064
33
WYR002 Weyers Acrofacial Dysostosis 36 0.064
34
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 35 0.064
35
BRD005 Borderline Leprosy 33 0.064
36
P SMT004 Smith-Lemli-Opitz Syndrome 84 0.045
37
P ALG002 Alagille Syndrome 83 0.045
38
BLM001 Bloom Syndrome 82 0.045
39
CLD001 Cleidocranial Dysplasia 78 0.045
40
PRG004 Progeria 77 0.045
41
LRN002 Laron Syndrome 76 0.045
42
OCL005 Oculocerebrorenal Syndrome 73 0.045
43
P CNG026 Congenital Heart Defect 73 0.045
44
CFF002 Coffin-Lowry Syndrome 70 0.045
45
CHR003 Cherubism 68 0.045
46
P RTH001 Rothmund-Thomson Syndrome 67 0.045
47
GNG013 Gingivitis 67 0.045
48
c CRN037 Craniosynostosis 67 0.045
49
LDD001 Ladd Syndrome 66 0.045
50
FCL009 Focal Dermal Hypoplasia 65 0.045
51
WLF001 Wolff-Parkinson-White Syndrome 65 0.045
52
ELL001 Ellis-Van Creveld Syndrome 64 0.045
53
c EPD003 Epidermolysis Bullosa Simplex 63 0.045
54
CLB001 Coloboma 63 0.045
55
SMT015 Smith Magenis Syndrome 62 0.045
56
P WVR001 Weaver Syndrome 62 0.045
57
ALP008 Alopecia 60 0.045
58
WLF002 Wolf-Hirschhorn Syndrome 60 0.045
59
LRN003 Learning Disability 58 0.045
60
LKD001 Leukodystrophy 58 0.045
61
SNG010 Single Median Maxillary Central Incisor 57 0.045
62
P SHR002 Short Stature 57 0.045
63
SNS001 Sensorineural Hearing Loss 56 0.045
64
BRS002 Beare-Stevenson Cutis Gyrata Syndrome 56 0.045
65
PPL006 Papillon-Lefevre Disease 54 0.045
66
JHN001 Johanson-Blizzard Syndrome 53 0.045
67
KRT009 Keratosis 53 0.045
68
c CTR002 Cataract 53 0.045
69
CHN016 Cohen Syndrome 53 0.045
70
P FNC004 Fanconi Syndrome 53 0.045
71
P STC005 Stickler Syndrome Type 1 53 0.045
72
WLL001 Williams-Beuren Syndrome 52 0.045
73
HYP514 Hypogonadotropic Hypogonadism 8 with or Without Anosmia 52 0.045
74
OST044 Osteoglophonic Dysplasia 52 0.045
75
c SYN001 Syndactyly 52 0.045
76
BLC003 Bloch-Sulzberger Syndrome 52 0.045
77
BRN003 Branchiooculofacial Syndrome 50 0.045
78
ANK001 Ankylosis 50 0.045
79
SCH016 Schimke Immunoosseous Dysplasia 49 0.045
80
P CHN005 Choanal Atresia 49 0.045
81
P DNT009 Dentin Dysplasia 49 0.045
82
P AXN003 Axenfeld-Rieger Syndrome Type 1 49 0.045
83
P OCL013 Oculodentodigital Dysplasia 49 0.045
84
ULN003 Ulnar-Mammary Syndrome 48 0.045
85
c TYP003 Type I Ehlers-Danlos Syndrome 48 0.045
86
P CRN139 Cornelia De Lange Syndrome 1 47 0.045
87
P TRC071 Treacher Collins Syndrome 3 45 0.045
88
PRT093 Proteus Syndrome, Somatic 44 0.045
89
VND002 Van Der Woude Syndrome 43 0.045
90
ORL010 Oral-Facial-Digital Syndrome Type I 43 0.045
91
OTP005 Oto-Palato-Digital Syndrome Type 2 43 0.045
92
RTR008 Root Resorption 43 0.045
93
TTR016 Tetra-Amelia Syndrome 43 0.045
94
P MBS002 Moebius Syndrome 42 0.045
95
P CRN108 Cranioectodermal Dysplasia 1 42 0.045
96
SYN053 Syndromic Diarrhea 42 0.045
97
c MYP006 Myopia 41 0.045
98
HYP022 Hypohidrosis 41 0.045
99
P RBN011 Robinow Syndrome, Autosomal Dominant 40 0.045
100
OCL014 Oculofaciocardiodental Syndrome 40 0.045
101
HYP030 Hypoactive Sexual Desire Disorder 39 0.045
102
MLN014 Melnick-Needles Syndrome 39 0.045
103
P KBK002 Kabuki Syndrome 1 37 0.045
104
TTH001 Tooth Ankylosis 37 0.045
105
KBG001 Kbg Syndrome 36 0.045
106
P OPT051 Opitz Gbbb Syndrome, Type I 35 0.045
107
ECT042 Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/palate Syndrome 3 35 0.045
108
P MCR044 Microcephalic Osteodysplastic Primordial Dwarfism Type 2 35 0.045
109
ECT070 Ectodermal Dysplasia 1, Hypohidrotic, X-Linked 35 0.045
110
HNN001 Hennekam Syndrome 35 0.045
111
c RBN009 Robinow Syndrome, Autosomal Recessive 34 0.045
112
RPP001 Rapp-Hodgkin Syndrome 34 0.045
113
P SCK023 Seckel Syndrome Type 1 34 0.045
114
CHR101 Char Syndrome 34 0.045
115
ANK009 Ankyloblepharon-Ectodermal Defects-Cleft Lip/palate Syndrome 33 0.045
116
ZNC001 Zunich Neuroectodermal Syndrome 32 0.045
117
DFN017 Deafness Onychodystrophy Osteodystrophy and Mental Retardation Syndrome 31 0.045
118
12Q002 12q14 Microdeletion Syndrome 31 0.045
119
OLM001 Olmsted Syndrome 31 0.045
120
P CNG044 Congenital Deafness with Labyrinthine Aplasia, Microtia, and Microdontia 30 0.045
121
FGF001 Fgfr-Related Craniosynostosis Syndromes 30 0.045
122
P KLN006 Koolen-De Vries Syndrome 29 0.045
123
SBS006 Sebastian Syndrome 28 0.045
124
c ATS004 Autosomal Dominant Microcephaly 28 0.045
125
2Q3003 2q32q33 Microdeletion Syndrome 27 0.045
126
SYN016 Syndactyly Cenani Lenz Type 27 0.045
127
P ATS061 Autosomal Recessive Hypotrichosis 26 0.045
128
c ORF007 Orofaciodigital Syndrome 2 26 0.045
129
ZLT002 Zlotogora Syndrome 25 0.045
130
ODN009 Odontoonychodermal Dysplasia 25 0.045
131
EMS001 Eem Syndrome 24 0.045
132
ACR029 Acrofacial Dysostosis Catania Type 24 0.045
133
RCH006 Richieri Costa Pereira Syndrome 23 0.045
134
CRN224 Craniofaciofrontodigital Syndrome 23 0.045
135
MNT038 Mental Retardation, Epileptic Seizures, Hypogonadism and Hypogenitalism, Microcephaly, and Obesity 23 0.045
136
PRG079 Progeria - Short Stature - Pigmented Nevi 23 0.045
137
ICH026 Ichthyosis, Leukocyte Vacuoles, Alopecia, and Sclerosing Cholangitis 22 0.045
138
GRL002 Gorlin Chaudhry Moss Syndrome 21 0.045
139
HYP465 Hypoglossia - Hypodactyly 21 0.045
140
TRC048 Trichodental Syndrome 21 0.045
141
CRN190 Craniosynostosis - Fibular Aplasia 21 0.045
142
ODN015 Odontotrichomelic Syndrome 20 0.045
143
CRN049 Craniolenticulosutural Dysplasia 20 0.045
144
WLS004 Wilson-Turner Syndrome 20 0.045
145
CRN082 Craniofacial Dysostosis with Diaphyseal Hyperplasia 20 0.045
146
LWR007 Lowry Maclean Syndrome 20 0.045
147
MXL012 Maxillo-Nasal Dysplasia 19 0.045
148
AML038 Amelogenesis Imperfecta and Gingival Fibromatosis Syndrome 18 0.045
149
SHR027 Short Stature Wormian Bones Dextrocardia 18 0.045
150
ACR030 Acrofacial Dysostosis Palagonia Type 18 0.045
151
P OTD002 Otodental Syndrome 18 0.045
152
BLP009 Blepharonasofacial Malformation Syndrome 18 0.045
153
DRM020 Dermatoosteolysis Kirghizian Type 17 0.045
154
c DST072 Distal Monosomy 6p 17 0.045
155
OCL058 Oculodental Syndrome, Rutherfurd Type 17 0.045
156
ACR077 Acro-Oto-Ocular Syndrome 17 0.045
157
TBS002 Teebi Shaltout Syndrome 16 0.045
158
FCC002 Faciocardiorenal Syndrome 16 0.045
159
SPL038 Splenogonadal Fusion - Limb Defects - Micrognathia 16 0.045
160
OCL056 Oculoosteocutaneous Syndrome 16 0.045
161
PRG024 Progeroid Syndrome Petty Type 16 0.045
162
CRB056 Cerebellar Ataxia Ectodermal Dysplasia 16 0.045
163
TRC047 Tricho Retino Dento Digital Syndrome 16 0.045
164
P 19P001 19p13.12 Microdeletion Syndrome 15 0.045
165
ECT015 Ectodermal Dysplasia Berlin Type 15 0.045
166
DRM023 Dermoodontodysplasia 15 0.045
167
PLL004 Pallister W Syndrome 15 0.045
168
CNG240 Congenital Unilateral Hypoplasia of Depressor Anguli Oris 15 0.045
169
BKS002 Book Syndrome 15 0.045
170
NNR006 Non-Eruption of Teeth - Maxillary Hypoplasia - Genu Valgum 15 0.045
171
STR034 Stratton-Garcia-Young Syndrome 15 0.045
172
TRC057 Trichoodontoonychial Dysplasia 14 0.045
173
TRD002 Taurodontia Absent Teeth Sparse Hair 14 0.045
174
PLD002 Pilodental Dysplasia with Refractive Errors 14 0.045
175
AML012 Ameloonychohypohidrotic Syndrome 14 0.045
176
CRB135 Cerebro-Oculo-Nasal Syndrome 14 0.045
177
EXT038 Extrasystoles Short Stature Hyperpigmentation Microcephaly 13 0.045
178
ECT021 Ectodermal Dysplasia Trichoodontoonychial Type 13 0.045
179
PLY032 Polydactyly Postaxial Dental and Vertebral 13 0.045
180
PNH003 Pinheiro Freire-Maia Miranda Syndrome 13 0.045
181
LLS001 Lelis Syndrome 12 0.045
182
MCR174 Macrocephaly - Short Stature - Paraplegia 12 0.045
183
ARR032 Arrhinia - Choanal Atresia - Microphthalmia 12 0.045
184
ANK005 Ankyloblepharon Filiforme Imperforate Anus 11 0.045
185
CLF020 Cleft Palate Stapes Fixation Oligodontia 10 0.045
186
CLF030 Cleft Lip/palate - Deafness - Sacral Lipoma 10 0.045
187
CHR159 Charlie M Syndrome 10 0.045
188
ODN004 Odonto Onycho Dysplasia with Alopecia 10 0.045
189
STL004 Stoll Alembik Finck Syndrome 9 0.045
190
SYM015 Symptomatic Form of Coffin-Lowry Syndrome in Female Carriers 8 0.045
191
CRT029 Cortada Koussef Matsumoto Syndrome 8 0.045
192
INT225 Intellectual Deficit - Athetosis - Microphthalmia 8 0.045
193
ECT060 Ectodermal Dysplasia 11a, Hypohidrotic/hair/tooth Type 8 0.045
194
c ECT058 Ectodermal Dysplasia 11b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 7 0.045
195
HYP044 Hypotrichosis of Eyelid 6 0.045