Smell/Taste Diseases Category (214 diseases)


Including: Nose, Tongue, Olfactory, Taste, Gustatory, Chemical senses
See other categories (disease lists)

# Family MCID Name MIFTS
1 TRG007 Trigonobrachycephaly, Bulbous Bifid Nose, Micrognathia, and Abnormalities of the Hands and Feet 18
2 P BFD001 Bifid Nose 25
3 BFD002 Bifid Nose with or Without Anorectal and Renal Anomalies 23
4 OLF005 Olfactory Neuroblastoma 52
5 NSD001 Nose Disease 52
6 NSN001 Nose, Anomalous Shape of 9
7 OLF004 Olfactory Nerve Neoplasm 22
8 HRY006 Hairy Nose Tip 18
9 c BFD005 Bifid Nose, Autosomal Recessive 14
10 EVN003 Even-Plus Syndrome 25
11 ALR004 Alar Cleft, Isolated 18
12 P RHN004 Rhinitis 63
13 c CHR048 Chronic Rhinitis 40
14 BSM002 Bosma Arhinia Microphthalmia Syndrome 35
15 OLF002 Olfactory Groove Meningioma 24
16 NSL005 Nasal Cavity Olfactory Neuroblastoma 7
17 OLF003 Olfactory Neural Tumor 5
18 HYD018 Hydrocephalus Craniosynostosis Bifid Nose 2
19 ATM008 Autoimmune Disease of Eyes, Ear, Nose and Throat 30
20 RYN005 Raynaud Phenomenon 52
21 TNG004 Tongue Disease 41
22 PRB002 Proboscis Lateralis 13
23 ISL111 Isolated Arrhinia 13
24 FRN052 Frontonasal Dysplasia-Bifid Nose-Upper Limb Anomalies Syndrome 13
25 c BFD004 Bifid Nose, Autosomal Dominant 11
26 PLY086 Polyrrhinia 8
27 P DST002 Distal Arthrogryposis 59
28 LCR014 Lacrimoauriculodentodigital Syndrome 57
29 c ART120 Arthrogryposis, Distal, Type 3 52
30 P THR117 Three M Syndrome 1 51
31 c ART144 Arthrogryposis, Distal, Type 1a 50
32 c ART119 Arthrogryposis, Distal, Type 5 50
33 CHN065 Choanal Atresia, Posterior 46
34 c ART061 Arthrogryposis, Distal, Type 2a 45
35 c ART146 Arthrogryposis, Distal, Type 9 41
36 P GLP001 Geleophysic Dysplasia 36
37 c ART147 Arthrogryposis, Distal, Type 7 34
38 c GLP003 Geleophysic Dysplasia 1 33
39 c GLP004 Geleophysic Dysplasia 2 32
40 VND005 Van Den Ende-Gupta Syndrome 29
41 c ART112 Arthrogryposis, Distal, Type 10 29
42 c ART104 Arthrogryposis, Distal, Type 5d 28
43 c THR069 Three M Syndrome 2 26
44 c ART122 Arthrogryposis, Distal, Type 8 25
45 FCL078 Facial Dysmorphism, Lens Dislocation, Anterior Segment Abnormalities, and Spontaneous Filtering Blebs 24
46 c THR096 Three M Syndrome 3 24
47 c ART128 Arthrogryposis, Distal, Type 6 23
48 c ART131 Arthrogryposis, Distal, Type 4 22
49 SLN006 Silent Sinus Syndrome 20
50 c GLP007 Geleophysic Dysplasia 3 19
51 c ART060 Arthrogryposis, Distal, Type 1b 19
52 SPR065 Supernumerary Nostril 19
53 NSL020 Nasal Glial Heterotopia 17
54 NSL017 Nasolacrimal Duct Cyst 16
55 c ART054 Arthrogryposis, Distal, Type 2e 16
56 CRN192 Craniorhiny 15
57 NSL021 Nasal Encephalocele 11
58 ISL022 Isolated Congenital Nasal Pyriform Aperture Stenosis 6
59 CHN052 Choanal Atresia, Bilateral 6
60 INT285 Intractable Diarrhea-Choanal Atresia-Eye Anomalies Syndrome 5
61 CHN051 Choanal Atresia, Unilateral 5
62 SPR109 Supratip Dysplasia 4
63 HYP737 Hyperhidrosis, Gustatory 38
64 OLF001 Olfactory Nerve Disease 21
65 SPN248 Spondyloepimetaphyseal Dysplasia, Sponastrime Type 34
66 ARR002 Arrhinia 12
67 P FRN036 Frontonasal Dysplasia 1 41
68 RPD002 Rapadilino Syndrome 39
69 c FRN033 Frontonasal Dysplasia 2 27
70 c FRN032 Frontonasal Dysplasia 3 25
71 c SX2003 Six2-Related Frontonasal Dysplasia 17
72 CMM005 Common Cold 62
73 c HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 58
74 WLF002 Wolf-Hirschhorn Syndrome 52
75 MRS002 Marshall Syndrome 45
76 c HYP513 Hypogonadotropic Hypogonadism 1 with or Without Anosmia 41
77 c HYP763 Hypogonadotropic Hypogonadism 23 Without Anosmia 41
78 c HYP548 Hypogonadotropic Hypogonadism 2 with or Without Anosmia 33
79 P HYP647 Hypogonadotropic Hypogonadism 24 Without Anosmia 30
80 c HYP565 Hypogonadotropic Hypogonadism 3 with or Without Anosmia 29
81 c HYP531 Hypogonadotropic Hypogonadism 4 with or Without Anosmia 28
82 c HYP547 Hypogonadotropic Hypogonadism 12 with or Without Anosmia 27
83 c HYP444 Hypogonadotropic Hypogonadism 9 with or Without Anosmia 25
84 c HYP552 Hypogonadotropic Hypogonadism 6 with or Without Anosmia 24
85 c HYP514 Hypogonadotropic Hypogonadism 8 with or Without Anosmia 24
86 c HYP532 Hypogonadotropic Hypogonadism 18 with or Without Anosmia 24
87 c HYP549 Hypogonadotropic Hypogonadism 5 with or Without Anosmia 24
88 c HYP511 Hypogonadotropic Hypogonadism 15 with or Without Anosmia 23
89 c HYP443 Hypogonadotropic Hypogonadism 13 with or Without Anosmia 22
90 c HYP817 Hypogonadotropic Hypogonadism 21 with or Without Anosmia 22
91 c HYP820 Hypogonadotropic Hypogonadism 22 with or Without Anosmia 22
92 c HYP518 Hypogonadotropic Hypogonadism 16 with or Without Anosmia 22
93 c HYP546 Hypogonadotropic Hypogonadism 20 with or Without Anosmia 22
94 c HYP521 Hypogonadotropic Hypogonadism 10 with or Without Anosmia 22
95 c HYP522 Hypogonadotropic Hypogonadism 11 with or Without Anosmia 22
96 c HYP523 Hypogonadotropic Hypogonadism 14 with or Without Anosmia 21
97 c HYP538 Hypogonadotropic Hypogonadism 17 with or Without Anosmia 21
98 c HYP557 Hypogonadotropic Hypogonadism 19 with or Without Anosmia 21
99 HRN021 Hernández-Aguirre Negrete Syndrome 13
100 VLJ001 Viljoen Kallis Voges Syndrome 11
101 ARH001 Arhinia Choanal Atresia Microphthalmia 10
102 P INF038 Influenza 75
103 ALL003 Allergic Rhinitis 69
104 P KLL001 Kallmann Syndrome 64
105 P SNS014 Sinusitis 64
106 RSC001 Rosacea 61
107 c RBN021 Rubinstein-Taybi Syndrome 1 48
108 BWN001 Bowen-Conradi Syndrome 43
109 c FRN011 Frontal Sinusitis 32
110 c RBN008 Rubinstein-Taybi Syndrome 2 29
111 c ACT035 Acute Frontal Sinusitis 20
112 c CHR040 Chronic Frontal Sinusitis 19
113 DWR018 Dwarfism, Levi Type 12
114 c KLL008 Kallmann Syndrome 6 10
115 c INF136 Influenza, Severe 9
116 CRM008 Crumpled Helices and Small Mouth 9
117 c KLL005 Kallmann Syndrome 3 9
118 c KLL006 Kallmann Syndrome 4 9
119 c KLL007 Kallmann Syndrome 5 8
120 P RBN007 Rubinstein Taybi Like Syndrome 7
121 MLN017 Milner Khallouf Gibson Syndrome 5
122 MSL001 Measles 66
123 P SCK004 Seckel Syndrome 54
124 CRT017 Cartilage Disease 52
125 P FBR025 Fibrochondrogenesis 50
126 c RBN009 Robinow Syndrome, Autosomal Recessive 47
127 P RBN002 Robinow Syndrome 46
128 c RBN017 Robinow Syndrome, Autosomal Dominant 2 46
129 c SCK009 Seckel Syndrome 1 45
130 c ATS082 Autosomal Dominant Robinow Syndrome 45
131 LCR013 Lacrimal Duct Defect 42
132 c RBN018 Robinow Syndrome, Autosomal Dominant 1 42
133 c SCK015 Seckel Syndrome 2 40
134 c VNM003 Van Maldergem Syndrome 1 39
135 c RBN020 Robinow Syndrome, Autosomal Dominant 3 37
136 TMP012 Temple Syndrome 35
137 SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 35
138 P OMD003 Omodysplasia 35
139 FMR018 Femoral-Facial Syndrome 34
140 c SCK011 Seckel Syndrome 5 30
141 MXL016 Maxillonasal Dysplasia, Binder Type 30
142 c SCK010 Seckel Syndrome 4 30
143 BRN062 Burn-Mckeown Syndrome 30
144 P VNM004 Van Maldergem Syndrome 29
145 c OMD001 Omodysplasia 1 29
146 NBL001 Nablus Mask-Like Facial Syndrome 29
147 HMC012 Hemicrania Continua 26
148 c OMD002 Omodysplasia 2 25
149 CHN040 Choanal Atresia and Lymphedema 25
150 c VNM002 Van Maldergem Syndrome 2 24
151 c SCK029 Seckel Syndrome 7 24
152 c FBR029 Fibrochondrogenesis 1 22
153 c SCK037 Seckel Syndrome 9 22
154 ANS017 Anosmia, Isolated Congenital 22
155 c SCK038 Seckel Syndrome 10 22
156 HYP212 Hypomandibular Faciocranial Dysostosis 21
157 BLP009 Blepharonasofacial Malformation Syndrome 21
158 c SCK033 Seckel Syndrome 8 21
159 c FBR030 Fibrochondrogenesis 2 19
160 SHR114 Short Stature, Facial Dysmorphism, and Skeletal Anomalies with or Without Cardiac Anomalies 19
161 c SCK032 Seckel Syndrome 6 18
162 RDL029 Radial Ray Hypoplasia with Choanal Atresia 17
163 c RR2001 Ror2-Related Robinow Syndrome 12
164 RNS001 Raine Syndrome 48
165 FLT006 Floating-Harbor Syndrome 45
166 CRN048 Craniofacial-Deafness-Hand Syndrome 29
167 c TRC091 Trichorhinophalangeal Syndrome, Type Ii 52
168 c TRC092 Trichorhinophalangeal Syndrome, Type I 46
169 c TRC093 Trichorhinophalangeal Syndrome, Type Iii 31
170 P TRC031 Trichorhinophalangeal Syndrome 28
171 c TRC104 Trichorhinophalangeal Syndrome Type 1 and 3 17
172 CRZ001 Crouzon Syndrome 70
173 HMF006 Hemifacial Microsomia 59
174 P ENC008 Encephalocele 48
175 OPS002 Opsismodysplasia 38
176 c BSL030 Basal Encephalocele 25
177 c FRN037 Frontal Encephalocele 24
178 JNS005 Jones Hersh Yusk Syndrome 9
179 PRT037 Pertussis 71
180 GLN010 Glanzmann Thrombasthenia 69
181 P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 65
182 HTC003 Hutchinson-Gilford Progeria Syndrome 65
183 FCT007 Factor Vii Deficiency 61
184 c BLD124 Bleeding Disorder, Platelet-Type, 11 55
185 MLN065 Melanocytic Nevus Syndrome, Congenital 54
186 FCT006 Factor V Deficiency 49
187 ACR013 Acrodysostosis 45
188 ACR041 Acromelic Frontonasal Dysostosis 40
189 c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 39
190 c BLD152 Bleeding Disorder, Platelet-Type, 16 34
191 SNN002 Sinonasal Undifferentiated Carcinoma 33
192 c BLD154 Bleeding Disorder, Platelet-Type, 12 31
193 c BLD156 Bleeding Disorder, Platelet-Type, 14 29
194 P BLD120 Bleeding Disorder, Platelet-Type, 8 25
195 c BLD125 Bleeding Disorder, Platelet-Type, 17 24
196 c BLD127 Bleeding Disorder, Platelet-Type, 19 24
197 c BLD121 Bleeding Disorder, Platelet-Type, 15 20
198 c BLD123 Bleeding Disorder, Platelet-Type, 13 20
199 c BLD132 Bleeding Disorder, Platelet-Type, 21 19
200 c BLD126 Bleeding Disorder, Platelet-Type, 18 19
201 c BLD133 Bleeding Disorder, Platelet-Type, 20 19
202 c BLD157 Bleeding Disorder, Platelet-Type, 9 19
203 FML079 Familial Nasal Acilia 11
204 P VNW001 Von Willebrand's Disease 63
205 c VNW010 Von Willebrand Disease, Type 2 56
206 DNN002 Donnai-Barrow Syndrome 55
207 c VNW008 Von Willebrand Disease, Type 3 52
208 ULN003 Ulnar-Mammary Syndrome 49
209 c VNW005 Von Willebrand Disease, Type 1 49
210 c ACQ017 Acquired Von Willebrand Syndrome 45
211 P OTS002 Otospondylomegaepiphyseal Dysplasia 44
212 c PSD048 Pseudo-Von Willebrand Disease 43
213 c OTS014 Otospondylomegaepiphyseal Dysplasia, Autosomal Dominant 43
214 c OTS013 Otospondylomegaepiphyseal Dysplasia, Autosomal Recessive 43



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