Smell/Taste Diseases Category (138 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 23
3 BFD002 Bifid Nose with or Without Anorectal and Renal Anomalies 24
4 OLF005 Olfactory Neuroblastoma 46
5 NSD001 Nose Disease 47
6 NSN001 Nose, Anomalous Shape of 9
7 OLF004 Olfactory Nerve Neoplasm 26
8 HRY006 Hairy Nose Tip 18
9 c BFD005 Bifid Nose, Autosomal Recessive 13
10 EVN003 Even-Plus Syndrome 25
11 ALR004 Alar Cleft, Isolated 18
12 P RHN004 Rhinitis 62
13 c CHR048 Chronic Rhinitis 41
14 BSM002 Bosma Arhinia Microphthalmia Syndrome 36
15 OLF002 Olfactory Groove Meningioma 30
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 35
20 RYN005 Raynaud Phenomenon 51
21 TNG004 Tongue Disease 43
22 PRB002 Proboscis Lateralis 13
23 ISL111 Isolated Arrhinia 13
24 c BFD004 Bifid Nose, Autosomal Dominant 12
25 PLY086 Polyrrhinia 8
26 FRN052 Frontonasal Dysplasia-Bifid Nose-Upper Limb Anomalies Syndrome 3
27 LCR014 Lacrimoauriculodentodigital Syndrome 59
28 P THR117 Three M Syndrome 1 52
29 CHN065 Choanal Atresia, Posterior 47
30 c GLP003 Geleophysic Dysplasia 1 33
31 VND005 Van Den Ende-Gupta Syndrome 29
32 FCL078 Facial Dysmorphism, Lens Dislocation, Anterior Segment Abnormalities, and Spontaneous Filtering Blebs 24
33 c THR096 Three M Syndrome 3 21
34 SLN006 Silent Sinus Syndrome 20
35 NSL017 Nasolacrimal Duct Cyst 19
36 SPR065 Supernumerary Nostril 19
37 c THR069 Three M Syndrome 2 19
38 c GLP007 Geleophysic Dysplasia 3 18
39 NSL020 Nasal Glial Heterotopia 17
40 CRN192 Craniorhiny 14
41 NSL021 Nasal Encephalocele 11
42 ISL022 Isolated Congenital Nasal Pyriform Aperture Stenosis 6
43 CHN052 Choanal Atresia, Bilateral 6
44 INT285 Intractable Diarrhea-Choanal Atresia-Eye Anomalies Syndrome 5
45 CHN051 Choanal Atresia, Unilateral 5
46 SPR109 Supratip Dysplasia 4
47 HYP737 Hyperhidrosis, Gustatory 38
48 OLF001 Olfactory Nerve Disease 13
49 ARR002 Arrhinia 12
50 SPN248 Spondyloepimetaphyseal Dysplasia, Sponastrime Type 31
51 CMM005 Common Cold 63
52 P FRN036 Frontonasal Dysplasia 1 42
53 c FRN033 Frontonasal Dysplasia 2 26
54 c FRN032 Frontonasal Dysplasia 3 25
55 c SX2003 Six2-Related Frontonasal Dysplasia 18
56 WLF002 Wolf-Hirschhorn Syndrome 53
57 MRS002 Marshall Syndrome 42
58 RPD002 Rapadilino Syndrome 39
59 HRN021 Hernández-Aguirre Negrete Syndrome 14
60 VLJ001 Viljoen Kallis Voges Syndrome 11
61 ARH001 Arhinia Choanal Atresia Microphthalmia 10
62 P INF038 Influenza 76
63 ALL003 Allergic Rhinitis 70
64 MSL001 Measles 65
65 P KLL001 Kallmann Syndrome 64
66 P SNS014 Sinusitis 63
67 RSC001 Rosacea 60
68 BWN001 Bowen-Conradi Syndrome 51
69 c FRN011 Frontal Sinusitis 30
70 c ACT035 Acute Frontal Sinusitis 21
71 c CHR040 Chronic Frontal Sinusitis 18
72 c INF136 Influenza, Severe 13
73 DWR018 Dwarfism, Levi Type 12
74 c KLL008 Kallmann Syndrome 6 11
75 c KLL006 Kallmann Syndrome 4 10
76 c KLL005 Kallmann Syndrome 3 10
77 c KLL007 Kallmann Syndrome 5 9
78 CRM008 Crumpled Helices and Small Mouth 6
79 MLN017 Milner Khallouf Gibson Syndrome 5
80 P ALC004 Alcohol Abuse 69
81 P FBR025 Fibrochondrogenesis 50
82 c SCK009 Seckel Syndrome 1 47
83 LCR013 Lacrimal Duct Defect 43
84 c SCK015 Seckel Syndrome 2 40
85 MXL016 Maxillonasal Dysplasia, Binder Type 39
86 SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 36
87 FMR018 Femoral-Facial Syndrome 35
88 TMP012 Temple Syndrome 35
89 P OMD003 Omodysplasia 33
90 c SCK011 Seckel Syndrome 5 31
91 c OMD001 Omodysplasia 1 31
92 c SCK010 Seckel Syndrome 4 30
93 BRN062 Burn-Mckeown Syndrome 30
94 NBL001 Nablus Mask-Like Facial Syndrome 29
95 CHN040 Choanal Atresia and Lymphedema 28
96 HMC012 Hemicrania Continua 27
97 c OMD002 Omodysplasia 2 26
98 c ALC016 Alcohol Sensitivity, Acute 23
99 c FBR029 Fibrochondrogenesis 1 23
100 ANS017 Anosmia, Isolated Congenital 22
101 c SCK033 Seckel Syndrome 8 22
102 HYP212 Hypomandibular Faciocranial Dysostosis 21
103 BLP009 Blepharonasofacial Malformation Syndrome 21
104 SHR114 Short Stature, Facial Dysmorphism, and Skeletal Anomalies with or Without Cardiac Anomalies 20
105 c FBR030 Fibrochondrogenesis 2 19
106 RDL029 Radial Ray Hypoplasia with Choanal Atresia 17
107 FLT006 Floating-Harbor Syndrome 45
108 RNS001 Raine Syndrome 45
109 CRN048 Craniofacial-Deafness-Hand Syndrome 29
110 c TRC091 Trichorhinophalangeal Syndrome, Type Ii 50
111 c TRC092 Trichorhinophalangeal Syndrome, Type I 48
112 P TRC031 Trichorhinophalangeal Syndrome 28
113 c TRC093 Trichorhinophalangeal Syndrome, Type Iii 26
114 c TRC104 Trichorhinophalangeal Syndrome Type 1 and 3 17
115 CRZ001 Crouzon Syndrome 65
116 P ENC008 Encephalocele 45
117 OPS002 Opsismodysplasia 38
118 c BSL030 Basal Encephalocele 26
119 c FRN037 Frontal Encephalocele 25
120 JNS005 Jones Hersh Yusk Syndrome 10
121 PRT037 Pertussis 68
122 GLN010 Glanzmann Thrombasthenia 68
123 HTC003 Hutchinson-Gilford Progeria Syndrome 65
124 P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 63
125 FCT007 Factor Vii Deficiency 61
126 HMF006 Hemifacial Microsomia 58
127 FCT006 Factor V Deficiency 55
128 MLN065 Melanocytic Nevus Syndrome, Congenital 54
129 c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 52
130 ACR041 Acromelic Frontonasal Dysostosis 48
131 ACR013 Acrodysostosis 46
132 SNN002 Sinonasal Undifferentiated Carcinoma 28
133 FML079 Familial Nasal Acilia 11
134 DNN002 Donnai-Barrow Syndrome 55
135 c OTS014 Otospondylomegaepiphyseal Dysplasia, Autosomal Dominant 52
136 ULN003 Ulnar-Mammary Syndrome 50
137 P OTS002 Otospondylomegaepiphyseal Dysplasia 46
138 c OTS013 Otospondylomegaepiphyseal Dysplasia, Autosomal Recessive 45



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