Smell/Taste Diseases Category (73 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 16
2 BFD001 Bifid Nose 26
3 BFD002 Bifid Nose with or Without Anorectal and Renal Anomalies 23
4 OLF005 Olfactory Neuroblastoma 43
5 NSD001 Nose Disease 49
6 PTT024 Potato Nose 9
7 OLF004 Olfactory Nerve Neoplasm 27
8 HRY006 Hairy Nose Tip 5
9 BSM002 Bosma Arhinia Microphthalmia Syndrome 30
10 OLF002 Olfactory Groove Meningioma 25
11 NSL005 Nasal Cavity Olfactory Neuroblastoma 15
12 MNT015 Mental Retardation Epilepsy Bulbous Nose 3
13 HYD018 Hydrocephalus Craniosynostosis Bifid Nose 2
14 P RHN004 Rhinitis 59
15 c CHR048 Chronic Rhinitis 39
16 EVN003 Even-Plus Syndrome 22
17 ATM008 Autoimmune Disease of Eyes, Ear, Nose and Throat 9
18 TNG004 Tongue Disease 41
19 PRB002 Proboscis Lateralis 12
20 HRN021 Hernández-Aguirre Negrete Syndrome 11
21 PRM135 Paramedian Nasal Cleft 6
22 ISL111 Isolated Arrhinia 6
23 PLY086 Polyrrhinia 6
24 OLF003 Olfactory Neural Tumor 4
25 CHN065 Choanal Atresia, Posterior 33
26 SPR065 Supernumerary Nostril 20
27 SLN006 Silent Sinus Syndrome 19
28 NSL017 Nasolacrimal Duct Cyst 14
29 CRN192 Craniorhiny 12
30 NSL020 Nasal Glial Heterotopia 12
31 NSL021 Nasal Encephalocele 11
32 INT285 Intractable Diarrhea-Choanal Atresia-Eye Anomalies Syndrome 5
33 CHN052 Choanal Atresia, Bilateral 4
34 CNG227 Congenital Nasal Pyriform Aperture Stenosis with Holoprosencephaly 4
35 CHN051 Choanal Atresia, Unilateral 4
36 SPR109 Supratip Dysplasia 4
37 OLF001 Olfactory Nerve Disease 19
38 FRY001 Frey Syndrome 35
39 c ZMM002 Zimmermann-Laband Syndrome 1 32
40 P ZMM001 Zimmermann-Laband Syndrome 26
41 c ZMM003 Zimmermann-Laband Syndrome 2 19
42 ARR002 Arrhinia 10
43 WLF002 Wolf-Hirschhorn Syndrome 50
44 MRS002 Marshall Syndrome 50
45 RPD002 Rapadilino Syndrome 40
46 HYP513 Hypogonadotropic Hypogonadism 1 with or Without Anosmia 38
47 VLJ001 Viljoen Kallis Voges Syndrome 9
48 ARH001 Arhinia Choanal Atresia Microphthalmia 7
49 P KLL001 Kallmann Syndrome 62
50 c RBN021 Rubinstein-Taybi Syndrome 1 32
51 c RBN008 Rubinstein-Taybi Syndrome 2 28
52 SPN248 Spondyloepimetaphyseal Dysplasia, Sponastrime Type 24
53 c KLL005 Kallmann Syndrome 3 18
54 c KLL007 Kallmann Syndrome 5 16
55 c KLL006 Kallmann Syndrome 4 15
56 c KLL008 Kallmann Syndrome 6 14
57 DWR007 Dwarfism Levi Type 9
58 P RBN007 Rubinstein Taybi Like Syndrome 9
59 c EP3001 Ep300-Related Rubinstein-Taybi Syndrome 8
60 c CRB084 Crebbp-Related Rubinstein-Taybi Syndrome 7
61 MLN017 Milner Khallouf Gibson Syndrome 4
62 CRM008 Crumpled Helices and Small Mouth 3
63 LDD001 Ladd Syndrome 60
64 LCR013 Lacrimal Duct Defect 22
65 CHN040 Choanal Atresia and Lymphedema 18
66 BLP009 Blepharonasofacial Malformation Syndrome 18
67 ANS017 Anosmia, Isolated Congenital 16
68 RDL029 Radial Ray Hypoplasia with Choanal Atresia 15
69 FLT006 Floating-Harbor Syndrome 44
70 RNS001 Raine Syndrome 44
71 CRN048 Craniofacial-Deafness-Hand Syndrome 30
72 JNS005 Jones Hersh Yusk Syndrome 7
73 FML079 Familial Nasal Acilia 10



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