Search results for "hypodontia"

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

204 hits were found for 'hypodontia'

# Family MCID Name MIFTS Score
1
MCR072 Microdontia Hypodontia Short Stature 4 3.999
2
PLR009 Pol Iii-Related Leukodystrophies 51 3.980
3
HYP196 Hypodontia, X-Linked 2 3.959
4
SCH038 Schopf-Schulz-Passarge Syndrome 29 3.452
5
EPD051 Epidermolysis Bullosa Simplex with Anodontia/hypodontia 16 3.452
6
TTH003 Tooth and Nail Syndrome 30 2.872
7
ECT063 Ectodermal Dysplasia 3, Witkop Type 22 2.828
8
CNG098 Congenital Heart Disease Ptosis Hypodontia Craniostosis 2 2.828
9
HYP195 Hypodontia of Incisors and Premolars 1 2.799
10
TTH002 Tooth Agenesis 37 2.108
11
ADL002 Adult Syndrome 41 2.044
12
DFN015 Deafness Oligodontia Syndrome 15 2.016
13
c AXN002 Axenfeld-Rieger Syndrome 66 1.979
14
MHT001 Mehta Lewis Patton Syndrome 3 1.979
15
ZDK001 Zadik Barak Levin Syndrome 2 1.979
16
ECT006 Ectodermal Dysplasia 49 0.141
17
c HYP087 Hypotrichosis 41 0.109
18
HYP013 Hypohidrotic Ectodermal Dysplasia 62 0.099
19
c AML002 Amelogenesis Imperfecta 46 0.089
20
TTH016 Tooth Agenesis, Selective, 1, with or Without Orofacial Cleft 40 0.089
21
TRD003 Taurodontism 34 0.089
22
P HYP080 Hypogonadism 59 0.077
23
VND002 Van Der Woude Syndrome 54 0.077
24
ECT061 Ectodermal Dysplasia 10a, Hypohidrotic/hair/nail Type, Autosomal Dominant 41 0.077
25
HYP064 Hypogonadotropism 39 0.077
26
DWN001 Down Syndrome 61 0.063
27
CLF001 Cleft Lip 59 0.063
28
EPD016 Epidermolysis Bullosa 56 0.063
29
P CLF002 Cleft Palate 52 0.063
30
P STR020 Strabismus 51 0.063
31
c STS001 Sotos Syndrome 49 0.063
32
OTP004 Oto-Palato-Digital Syndrome Type 1 40 0.063
33
AND001 Anodontia 39 0.063
34
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 33 0.063
35
P SMT004 Smith-Lemli-Opitz Syndrome 82 0.044
36
P ALG002 Alagille Syndrome 80 0.044
37
CLD001 Cleidocranial Dysplasia 77 0.044
38
LRN002 Laron Syndrome 76 0.044
39
SKN016 Skin Disease 75 0.044
40
BLM001 Bloom Syndrome 74 0.044
41
PRG004 Progeria 72 0.044
42
CFF002 Coffin-Lowry Syndrome 72 0.044
43
WLF001 Wolff-Parkinson-White Syndrome 70 0.044
44
c CRN037 Craniosynostosis 70 0.044
45
OCL005 Oculocerebrorenal Syndrome 69 0.044
46
P RTH001 Rothmund-Thomson Syndrome 68 0.044
47
CHR003 Cherubism 67 0.044
48
P SHR002 Short Stature 64 0.044
49
CLB001 Coloboma 64 0.044
50
LRN003 Learning Disability 62 0.044
51
c EPD003 Epidermolysis Bullosa Simplex 62 0.044
52
GNG013 Gingivitis 62 0.044
53
LDD001 Ladd Syndrome 61 0.044
54
P FRS003 Fraser Syndrome 60 0.044
55
ELL001 Ellis-Van Creveld Syndrome 60 0.044
56
SNG010 Single Median Maxillary Central Incisor 60 0.044
57
WLF002 Wolf-Hirschhorn Syndrome 59 0.044
58
P CNG401 Congenital Heart Disease 58 0.044
59
FCL009 Focal Dermal Hypoplasia 57 0.044
60
SNS001 Sensorineural Hearing Loss 57 0.044
61
ANK001 Ankylosis 57 0.044
62
c CTR002 Cataract 57 0.044
63
ALP008 Alopecia 56 0.044
64
SMT015 Smith Magenis Syndrome 56 0.044
65
P WVR001 Weaver Syndrome 56 0.044
66
BRS002 Beare-Stevenson Cutis Gyrata Syndrome 55 0.044
67
OST044 Osteoglophonic Dysplasia 55 0.044
68
P OCL013 Oculodentodigital Dysplasia 55 0.044
69
WLL001 Williams-Beuren Syndrome 54 0.044
70
JHN001 Johanson-Blizzard Syndrome 53 0.044
71
MBS002 Moebius Syndrome 53 0.044
72
HYP514 Hypogonadotropic Hypogonadism 8 with or Without Anosmia 53 0.044
73
LKD001 Leukodystrophy 52 0.044
74
ULN003 Ulnar-Mammary Syndrome 52 0.044
75
MNT147 Mental Retardation 51 0.044
76
c SYN001 Syndactyly 50 0.044
77
BLC003 Bloch-Sulzberger Syndrome 50 0.044
78
CHN016 Cohen Syndrome 50 0.044
79
P FNC004 Fanconi Syndrome 49 0.044
80
KRT009 Keratosis 49 0.044
81
P AXN003 Axenfeld-Rieger Syndrome Type 1 49 0.044
82
P CRN139 Cornelia De Lange Syndrome 1 47 0.044
83
P TRC071 Treacher Collins Syndrome 3 47 0.044
84
CHN005 Choanal Atresia 47 0.044
85
SCH016 Schimke Immunoosseous Dysplasia 46 0.044
86
BRN003 Branchiooculofacial Syndrome 46 0.044
87
PRT093 Proteus Syndrome, Somatic 45 0.044
88
KRT012 Keratoderma 45 0.044
89
MLN014 Melnick-Needles Syndrome 44 0.044
90
PPL006 Papillon-Lefevre Disease 44 0.044
91
P STC005 Stickler Syndrome Type 1 44 0.044
92
PRR010 Pierre Robin Sequence 43 0.044
93
HYP022 Hypohidrosis 43 0.044
94
OCL014 Oculofaciocardiodental Syndrome 43 0.044
95
RPP001 Rapp-Hodgkin Syndrome 43 0.044
96
ORL010 Oral-Facial-Digital Syndrome Type I 42 0.044
97
TTR016 Tetra-Amelia Syndrome 41 0.044
98
P MYH004 Myh9 Related Thrombocytopenia 41 0.044
99
P CRN108 Cranioectodermal Dysplasia 1 41 0.044
100
OTP005 Oto-Palato-Digital Syndrome Type 2 40 0.044
101
c MYP006 Myopia 40 0.044
102
SPL040 Split Hand 40 0.044
103
HNN001 Hennekam Syndrome 39 0.044
104
c TYP003 Type I Ehlers-Danlos Syndrome 39 0.044
105
ACT164 Actinic Prurigo 39 0.044
106
P SCK028 Seckel Syndrome Type 8 38 0.044
107
SPL039 Split Foot 38 0.044
108
PLT008 Pili Torti 38 0.044
109
TTH001 Tooth Ankylosis 38 0.044
110
KBG001 Kbg Syndrome 38 0.044
111
WYR002 Weyers Acrofacial Dysostosis 38 0.044
112
OLM001 Olmsted Syndrome 37 0.044
113
RTR008 Root Resorption 36 0.044
114
P KBK002 Kabuki Syndrome 1 36 0.044
115
P MCR044 Microcephalic Osteodysplastic Primordial Dwarfism Type 2 34 0.044
116
FGF001 Fgfr-Related Craniosynostosis Syndromes 33 0.044
117
BRD005 Borderline Leprosy 33 0.044
118
NLX001 Neu Laxova Syndrome 33 0.044
119
P OPT051 Opitz Gbbb Syndrome, Type I 33 0.044
120
ECT042 Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/palate Syndrome 3 32 0.044
121
ANK009 Ankyloblepharon-Ectodermal Defects-Cleft Lip/palate Syndrome 32 0.044
122
YNS001 Yunis Varon Syndrome 32 0.044
123
ECT070 Ectodermal Dysplasia 1, Hypohidrotic, X-Linked 32 0.044
124
SYN053 Syndromic Diarrhea 32 0.044
125
P RBN011 Robinow Syndrome, Autosomal Dominant 32 0.044
126
ZNC001 Zunich Neuroectodermal Syndrome 31 0.044
127
P ATS061 Autosomal Recessive Hypotrichosis 31 0.044
128
ODN006 Odontoma 31 0.044
129
c RBN009 Robinow Syndrome, Autosomal Recessive 31 0.044
130
P KLN008 Koolen De Vries Syndrome 30 0.044
131
P MYP018 Myopia 6 30 0.044
132
c ATS004 Autosomal Dominant Microcephaly 30 0.044
133
CHR101 Char Syndrome 30 0.044
134
EMS001 Eem Syndrome 30 0.044
135
DFN017 Deafness Onychodystrophy Osteodystrophy and Mental Retardation Syndrome 29 0.044
136
12Q002 12q14 Microdeletion Syndrome 28 0.044
137
ODN009 Odontoonychodermal Dysplasia 28 0.044
138
RCH006 Richieri Costa Pereira Syndrome 28 0.044
139
c ORF007 Orofaciodigital Syndrome 2 27 0.044
140
P OTD002 Otodental Syndrome 26 0.044
141
ZLT002 Zlotogora Syndrome 26 0.044
142
P CNG044 Congenital Deafness with Labyrinthine Aplasia, Microtia, and Microdontia 26 0.044
143
HYP465 Hypoglossia - Hypodactyly 26 0.044
144
SYN016 Syndactyly Cenani Lenz Type 26 0.044
145
GRL002 Gorlin Chaudhry Moss Syndrome 25 0.044
146
ACR029 Acrofacial Dysostosis Catania Type 24 0.044
147
MNT038 Mental Retardation, Epileptic Seizures, Hypogonadism and Hypogenitalism, Microcephaly, and Obesity 23 0.044
148
ICH026 Ichthyosis, Leukocyte Vacuoles, Alopecia, and Sclerosing Cholangitis 23 0.044
149
ODN015 Odontotrichomelic Syndrome 22 0.044
150
LWR007 Lowry Maclean Syndrome 22 0.044
151
MXL012 Maxillo-Nasal Dysplasia 22 0.044
152
TRC048 Trichodental Syndrome 22 0.044
153
CRN190 Craniosynostosis - Fibular Aplasia 20 0.044
154
CRN082 Craniofacial Dysostosis with Diaphyseal Hyperplasia 20 0.044
155
CRN049 Craniolenticulosutural Dysplasia 20 0.044
156
PRG098 Progéria - Short Stature - Pigmented Nevi 20 0.044
157
WLS004 Wilson-Turner Syndrome 20 0.044
158
ACR030 Acrofacial Dysostosis Palagonia Type 20 0.044
159
DRM023 Dermoodontodysplasia 19 0.044
160
SHR027 Short Stature Wormian Bones Dextrocardia 19 0.044
161
TBS002 Teebi Shaltout Syndrome 19 0.044
162
GLS018 Glass Syndrome 19 0.044
163
CRN224 Craniofaciofrontodigital Syndrome 18 0.044
164
ACR077 Acro-Oto-Ocular Syndrome 18 0.044
165
BLP009 Blepharonasofacial Malformation Syndrome 18 0.044
166
c DST072 Distal Monosomy 6p 18 0.044
167
FCC002 Faciocardiorenal Syndrome 17 0.044
168
DRM020 Dermatoosteolysis Kirghizian Type 17 0.044
169
CRB135 Cerebro-Oculo-Nasal Syndrome 17 0.044
170
OCL058 Oculodental Syndrome, Rutherfurd Type 17 0.044
171
PRG024 Progeroid Syndrome Petty Type 17 0.044
172
P 19P001 19p13.12 Microdeletion Syndrome 17 0.044
173
CNG240 Congenital Unilateral Hypoplasia of Depressor Anguli Oris 16 0.044
174
CRB056 Cerebellar Ataxia Ectodermal Dysplasia 16 0.044
175
PLL004 Pallister W Syndrome 16 0.044
176
BKS002 Book Syndrome 16 0.044
177
SPL038 Splenogonadal Fusion - Limb Defects - Micrognathia 16 0.044
178
LLS001 Lelis Syndrome 16 0.044
179
TRC047 Tricho Retino Dento Digital Syndrome 16 0.044
180
ECT015 Ectodermal Dysplasia Berlin Type 16 0.044
181
AML012 Ameloonychohypohidrotic Syndrome 15 0.044
182
NNR006 Non-Eruption of Teeth - Maxillary Hypoplasia - Genu Valgum 15 0.044
183
PLD002 Pilodental Dysplasia with Refractive Errors 15 0.044
184
OCL056 Oculoosteocutaneous Syndrome 15 0.044
185
TRD002 Taurodontia Absent Teeth Sparse Hair 15 0.044
186
EXT038 Extrasystoles Short Stature Hyperpigmentation Microcephaly 14 0.044
187
PLY032 Polydactyly Postaxial Dental and Vertebral 14 0.044
188
CRN113 Craniosynostosis, Syndromic 14 0.044
189
TRC057 Trichoodontoonychial Dysplasia 14 0.044
190
ECT021 Ectodermal Dysplasia Trichoodontoonychial Type 13 0.044
191
PNH003 Pinheiro Freire-Maia Miranda Syndrome 13 0.044
192
MCR174 Macrocephaly - Short Stature - Paraplegia 12 0.044
193
CLF020 Cleft Palate Stapes Fixation Oligodontia 12 0.044
194
ARR032 Arrhinia - Choanal Atresia - Microphthalmia 11 0.044
195
BRC077 Brachydactyly - Mesomelia - Intellectual Disability - Heart Defects 11 0.044
196
ANK005 Ankyloblepharon Filiforme Imperforate Anus 11 0.044
197
STL004 Stoll Alembik Finck Syndrome 11 0.044
198
CHR159 Charlie M Syndrome 10 0.044
199
ODN004 Odonto Onycho Dysplasia with Alopecia 10 0.044
200
CLF030 Cleft Lip/palate - Deafness - Sacral Lipoma 10 0.044
201
c ECT058 Ectodermal Dysplasia 11b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 9 0.044
202
INT231 Intellectual Disability - Athetosis - Microphthalmia 9 0.044
203
SYM015 Symptomatic Form of Coffin-Lowry Syndrome in Female Carriers 8 0.044
204
ECT060 Ectodermal Dysplasia 11a, Hypohidrotic/hair/tooth Type 8 0.044