Smell/Taste Diseases Category (267 diseases)


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

# Family MCID Name MIFTS
1 FSS001 Fissured Tongue 30
2 HYP737 Hyperhidrosis, Gustatory 37
3 TNG004 Tongue Disease 43
4 TRG007 Trigonobrachycephaly, Bulbous Bifid Nose, Micrognathia, and Abnormalities of the Hands and Feet 17
5 OLF005 Olfactory Neuroblastoma 46
6 NSD001 Nose Disease 45
7 CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60
8 SPN248 Spondyloepimetaphyseal Dysplasia, Sponastrime Type 35
9 BTG003 Beta-Glucopyranoside Tasting 12
10 EVN003 Even-Plus Syndrome 27
11 c BFD005 Bifid Nose, Autosomal Recessive 11
12 THR113 Thiourea Tasting 19
13 RPD002 Rapadilino Syndrome 47
14 TNG009 Tongue Squamous Cell Carcinoma 43
15 ALR004 Alar Cleft, Isolated 16
16 ARR002 Arrhinia 12
17 NSL005 Nasal Cavity Olfactory Neuroblastoma 27
18 OLF002 Olfactory Groove Meningioma 22
19 NSN001 Nose, Anomalous Shape of 10
20 OLF003 Olfactory Neural Tumor 6
21 P RHN004 Rhinitis 57
22 c CHR048 Chronic Rhinitis 46
23 HRN021 Hernández-Aguirre Negrete Syndrome 13
24 c RBN021 Rubinstein-Taybi Syndrome 1 57
25 BWN001 Bowen-Conradi Syndrome 54
26 c RBN008 Rubinstein-Taybi Syndrome 2 38
27 P RBN007 Rubinstein Taybi Like Syndrome 20
28 DWR018 Dwarfism, Levi Type 12
29 FRN052 Frontonasal Dysplasia-Bifid Nose-Upper Limb Anomalies Syndrome 11
30 HRY006 Hairy Nose Tip 11
31 GGR002 Geographic and Fissured Tongue 11
32 c BFD004 Bifid Nose, Autosomal Dominant 10
33 TNG010 Tongue Curling, Folding, or Rolling 9
34 TNG011 Tongue, Pigmented Fungiform Papillae of 9
35 CRM008 Crumpled Helices and Small Mouth 8
36 ART145 Artichoke, Modification of Taste by 6
37 GNT157 Genetic Nose and Cavum Anomaly 2
38 P THR117 Three M Syndrome 1 64
39 P CFF008 Coffin-Siris Syndrome 1 63
40 CHN065 Choanal Atresia, Posterior 48
41 BRN062 Burn-Mckeown Syndrome 46
42 c CFF007 Coffin-Siris Syndrome 2 43
43 c CFF009 Coffin-Siris Syndrome 4 42
44 c CFF010 Coffin-Siris Syndrome 3 42
45 c CFF011 Coffin-Siris Syndrome 6 35
46 c CFF014 Coffin-Siris Syndrome 9 32
47 c THR069 Three M Syndrome 2 32
48 STP011 Stapes Ankylosis with Broad Thumbs and Toes 28
49 FCL078 Facial Dysmorphism, Lens Dislocation, Anterior Segment Abnormalities, and Spontaneous Filtering Blebs 28
50 HMC012 Hemicrania Continua 26
51 c CFF012 Coffin-Siris Syndrome 7 25
52 ANS017 Anosmia, Isolated Congenital 25
53 c CFF006 Coffin-Siris Syndrome 5 24
54 c CFF013 Coffin-Siris Syndrome 8 24
55 c THR096 Three M Syndrome 3 24
56 HYP865 Hypogonadotropic Hypogonadism 25 with Anosmia 23
57 HYP212 Hypomandibular Faciocranial Dysostosis 23
58 c CFF015 Coffin-Siris Syndrome 10 22
59 c CFF016 Coffin-Siris Syndrome 11 21
60 SLN006 Silent Sinus Syndrome 21
61 NSL017 Nasolacrimal Duct Cyst 18
62 NSL020 Nasal Glial Heterotopia 17
63 CHN052 Choanal Atresia, Bilateral 8
64 SPR109 Supratip Dysplasia 3
65 TNG007 Tongue Carcinoma 55
66 OLF001 Olfactory Nerve Disease 12
67 ANK020 Ankyloglossia with or Without Tooth Anomalies 46
68 P ZMM001 Zimmermann-Laband Syndrome 39
69 c ZMM002 Zimmermann-Laband Syndrome 1 34
70 HRY002 Hairy Tongue 28
71 c ZMM003 Zimmermann-Laband Syndrome 2 22
72 c ZMM004 Zimmermann-Laband Syndrome 3 21
73 DGS006 Digestive Duplication Cyst of the Tongue 8
74 MCR037 Macroglossia 44
75 GGR001 Geographic Tongue 38
76 OLF004 Olfactory Nerve Neoplasm 21
77 CRN048 Craniofacial-Deafness-Hand Syndrome 52
78 ATR073 Atrophic Glossitis 28
79 HYP049 Hypertrophy of Tongue Papillae 24
80 CLF036 Cleft Tongue 14
81 KYP007 Kyphoscoliosis-Lateral Tongue Atrophy-Hereditary Spastic Paraplegia Syndrome 13
82 c ORF037 Orofaciodigital Syndrome I 59
83 ORL004 Oral Submucous Fibrosis 56
84 c TRC092 Trichorhinophalangeal Syndrome, Type I 54
85 c TRC091 Trichorhinophalangeal Syndrome, Type Ii 51
86 P ORF001 Orofaciodigital Syndrome 50
87 c ORF035 Orofaciodigital Syndrome Iv 49
88 c ORF033 Orofaciodigital Syndrome V 43
89 P TRC031 Trichorhinophalangeal Syndrome 37
90 c ORF038 Orofaciodigital Syndrome Iii 36
91 c ORF036 Orofaciodigital Syndrome Xiv 31
92 c ORF041 Orofaciodigital Syndrome X 29
93 c ORF046 Orofaciodigital Syndrome Xvi 24
94 c ORF042 Orofaciodigital Syndrome Xi 24
95 c ORF052 Orofaciodigital Syndrome Xviii 23
96 c TRC104 Trichorhinophalangeal Syndrome Type 1 and 3 23
97 c ORF051 Orofaciodigital Syndrome Xvii 22
98 c ORF045 Orofaciodigital Syndrome Xv 21
99 c ORF039 Orofaciodigital Syndrome Vii 20
100 VLJ001 Viljoen Kallis Voges Syndrome 16
101 c ORF005 Orofaciodigital Syndrome 12 12
102 c ORF006 Orofaciodigital Syndrome 13 11
103 c MYP072 Myopathy, Myofibrillar, 1 55
104 P FBR025 Fibrochondrogenesis 55
105 BRN009 Burning Mouth Syndrome 51
106 c MYP078 Myopathy, Myofibrillar, 3 50
107 P MYF003 Myofibrillar Myopathy 50
108 c MYP079 Myopathy, Myofibrillar, 5 48
109 P ENC008 Encephalocele 46
110 c FBR029 Fibrochondrogenesis 1 45
111 KPR003 Keipert Syndrome 44
112 c MYP080 Myopathy, Myofibrillar, 4 43
113 c MYP081 Myopathy, Myofibrillar, 6 42
114 c MYP082 Myopathy, Myofibrillar, 2 40
115 CTL005 Catel-Manzke Syndrome 37
116 c MYP119 Myopathy, Myofibrillar, 7 33
117 c MYP118 Myopathy, Myofibrillar, 8 31
118 c FBR030 Fibrochondrogenesis 2 26
119 c FRN037 Frontal Encephalocele 25
120 c BSL030 Basal Encephalocele 24
121 c MYF011 Myofibrillar Myopathy 10 22
122 c MYF012 Myofibrillar Myopathy 11 18
123 JNS005 Jones Hersh Yusk Syndrome 9
124 MLN017 Milner Khallouf Gibson Syndrome 5
125 PHR003 Pharyngitis 57
126 c VNM003 Van Maldergem Syndrome 1 50
127 ORM002 Oromandibular Dystonia 41
128 c TRC093 Trichorhinophalangeal Syndrome, Type Iii 38
129 OPT010 Optic Papillitis 38
130 FCL011 Facial Nerve Disease 38
131 PSD001 Pseudobulbar Palsy 37
132 c VNM002 Van Maldergem Syndrome 2 35
133 HYP679 Hypoglossia-Hypodactylia 33
134 MXL016 Maxillonasal Dysplasia, Binder Type 31
135 P VNM004 Van Maldergem Syndrome 29
136 P SHR126 Short Stature, Facial Dysmorphism, and Skeletal Anomalies with or Without Cardiac Anomalies 2 24
137 SNS026 Sensory System Disease 22
138 c SHR125 Short Stature, Facial Dysmorphism, and Skeletal Anomalies with or Without Cardiac Anomalies 1 22
139 NSL021 Nasal Encephalocele 12
140 ISL022 Isolated Congenital Nasal Pyriform Aperture Stenosis 8
141 CHN051 Choanal Atresia, Unilateral 5
142 FLT006 Floating-Harbor Syndrome 52
143 BLL003 Bell's Palsy 48
144 ORL011 Oral Cancer 60
145 MLK003 Melkersson-Rosenthal Syndrome 43
146 ODN009 Odontoonychodermal Dysplasia 35
147 MNT006 Manitoba Oculotrichoanal Syndrome 35
148 MSL001 Measles 61
149 P PRR016 Pierre Robin Syndrome 50
150 VTM002 Vitamin B12 Deficiency 48
151 SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47
152 LTR003 Lateral Medullary Syndrome 35
153 c ORF043 Orofaciodigital Syndrome Ix 35
154 FMR018 Femoral-Facial Syndrome 31
155 c DNC007 Diencephalic-Mesencephalic Junction Dysplasia Syndrome 1 28
156 P NBS002 Nabais Sa-De Vries Syndrome, Type 2 23
157 c DNC008 Diencephalic-Mesencephalic Junction Dysplasia Syndrome 2 23
158 P DNC006 Diencephalic-Mesencephalic Junction Dysplasia 20
159 c NBS001 Nabais Sa-De Vries Syndrome, Type 1 20
160 SPR065 Supernumerary Nostril 17
161 CRN192 Craniorhiny 16
162 RDL029 Radial Ray Hypoplasia with Choanal Atresia 16
163 PRB002 Proboscis Lateralis 14
164 FML079 Familial Nasal Acilia 13
165 ISL111 Isolated Arrhinia 12
166 PLY086 Polyrrhinia 11
167 NSN002 Nose and Cavum Anomaly 6
168 c RRD018 Rare Disease with Pierre Robin Syndrome 4
169 OPS002 Opsismodysplasia 38
170 P BLD124 Bleeding Disorder, Platelet-Type, 11 68
171 c PCH015 Pachyonychia Congenita 1 60
172 P SCK004 Seckel Syndrome 58
173 OST044 Osteoglophonic Dysplasia 55
174 PRT037 Pertussis 49
175 c SCK009 Seckel Syndrome 1 48
176 CHL109 Childhood Apraxia of Speech 44
177 c PCH010 Pachyonychia Congenita 3 43
178 RPP001 Rapp-Hodgkin Syndrome 43
179 c SCK015 Seckel Syndrome 2 40
180 c PCH012 Pachyonychia Congenita 2 40
181 c BLD126 Bleeding Disorder, Platelet-Type, 18 39
182 ORL019 Oral Hairy Leukoplakia 39
183 c SCK011 Seckel Syndrome 5 39
184 P OMD003 Omodysplasia 38
185 TMP012 Temple Syndrome 38
186 c SCK010 Seckel Syndrome 4 38
187 c SCK029 Seckel Syndrome 7 36
188 c BLD152 Bleeding Disorder, Platelet-Type, 16 36
189 c BLD157 Bleeding Disorder, Platelet-Type, 9 36
190 c BLD120 Bleeding Disorder, Platelet-Type, 8 36
191 c BLD125 Bleeding Disorder, Platelet-Type, 17 36
192 c OMD001 Omodysplasia 1 35
193 c BLD156 Bleeding Disorder, Platelet-Type, 14 33
194 c SCK033 Seckel Syndrome 8 31
195 c SCK032 Seckel Syndrome 6 30
196 SNN002 Sinonasal Undifferentiated Carcinoma 30
197 c OMD002 Omodysplasia 2 28
198 c BLD154 Bleeding Disorder, Platelet-Type, 12 27
199 c BLD133 Bleeding Disorder, Platelet-Type, 20 27
200 c PCH011 Pachyonychia Congenita 4 26
201 c SCK037 Seckel Syndrome 9 24
202 c SCK038 Seckel Syndrome 10 23
203 c BLD127 Bleeding Disorder, Platelet-Type, 19 23
204 c BLD121 Bleeding Disorder, Platelet-Type, 15 22
205 c BLD132 Bleeding Disorder, Platelet-Type, 21 22
206 c BLD123 Bleeding Disorder, Platelet-Type, 13 22
207 c BLD168 Bleeding Disorder, Platelet-Type, 22 17
208 P PCH020 Pachyonychia Congenita, Autosomal Recessive 11
209 INT285 Intractable Diarrhea-Choanal Atresia-Eye Anomalies Syndrome 5
210 c NRP053 Neuropathy, Hereditary Sensory and Autonomic, Type Iia 67
211 GLN010 Glanzmann Thrombasthenia 66
212 c NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 66
213 c MLN065 Melanocytic Nevus Syndrome, Congenital 61
214 GST092 Gastroesophageal Reflux 60
215 c NRP037 Neuropathy, Hereditary Sensory and Autonomic, Type V 55
216 c ORF034 Orofaciodigital Syndrome Vi 55
217 ACR041 Acromelic Frontonasal Dysostosis 53
218 P LRG012 Large Congenital Melanocytic Nevus 47
219 c NRP031 Neuropathy, Hereditary Sensory and Autonomic, Type Vii 45
220 BSM002 Bosma Arhinia Microphthalmia Syndrome 45
221 c HRD201 Hereditary Sensory and Autonomic Neuropathy Type 1 44
222 c NRP033 Neuropathy, Hereditary Sensory and Autonomic, Type Ia 43
223 c NRP044 Neuropathy, Hereditary Sensory and Autonomic, Type Viii 43
224 c NRP040 Neuropathy, Hereditary Sensory and Autonomic, Type Ic 42
225 c NRP038 Neuropathy, Hereditary Sensory and Autonomic, Type Vi 42
226 LCR013 Lacrimal Duct Defect 40
227 c NRP018 Neuropathy, Hereditary Sensory and Autonomic, Type Iib 39
228 SCR015 Scarlet Fever 38
229 BFD002 Bifid Nose with or Without Anorectal and Renal Anomalies 27
230 OCL030 Oculoauriculofrontonasal Syndrome 24
231 P BFD001 Bifid Nose 20
232 c ATS273 Autosomal Recessive Hereditary Sensory and Autonomic Neuropathy 6
233 P ATS271 Autosomal Dominant Hereditary Sensory and Autonomic Neuropathy 5
234 CHN078 Choanal Atresia-Athelia-Hypothyroidism-Delayed Puberty-Short Stature Syndrome 4
235 P DST002 Distal Arthrogryposis 63
236 c ART144 Arthrogryposis, Distal, Type 1a 60
237 c ART061 Arthrogryposis, Distal, Type 2a 58
238 FCT006 Factor V Deficiency 55
239 ORP003 Oropharynx Cancer 54
240 c ART119 Arthrogryposis, Distal, Type 5 51
241 c ART120 Arthrogryposis, Distal, Type 3 49
242 c ART155 Arthrogryposis, Distal, Type 2b1 45
243 c ART147 Arthrogryposis, Distal, Type 7 44
244 c ART104 Arthrogryposis, Distal, Type 5d 41
245 VBR001 Vibratory Urticaria 37
246 c ART112 Arthrogryposis, Distal, Type 10 34
247 c ART060 Arthrogryposis, Distal, Type 1b 33
248 c ART131 Arthrogryposis, Distal, Type 4 28
249 c ART128 Arthrogryposis, Distal, Type 6 27
250 c ART157 Arthrogryposis, Distal, Type 2b3 25
251 c ART156 Arthrogryposis, Distal, Type 2b2 25
252 CHN040 Choanal Atresia and Lymphedema 21
253 c ART168 Arthrogryposis, Distal, Type 1c 19
254 c ART054 Arthrogryposis, Distal, Type 2e 14
255 P RBN002 Robinow Syndrome 55
256 c RBN022 Robinow Syndrome, Autosomal Recessive 1 55
257 c RBN018 Robinow Syndrome, Autosomal Dominant 1 50
258 c ATS082 Autosomal Dominant Robinow Syndrome 46
259 c RBN017 Robinow Syndrome, Autosomal Dominant 2 45
260 MNT237 Mental Retardation with Language Impairment and with or Without Autistic Features 41
261 c RBN020 Robinow Syndrome, Autosomal Dominant 3 34
262 c RBN023 Robinow Syndrome, Autosomal Recessive 2 25
263 BLP009 Blepharonasofacial Malformation Syndrome 23
264 c RR2001 Ror2-Related Robinow Syndrome 13
265 LCR014 Lacrimoauriculodentodigital Syndrome 58
266 CDS002 Codas Syndrome 44
267 c ORF040 Orofaciodigital Syndrome Viii 49



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