Smell/Taste Diseases Category (72 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	19
2		BFD001	Bifid Nose	22
3		BFD002	Bifid Nose with or Without Anorectal and Renal Anomalies	24
4		OLF005	Olfactory Neuroblastoma	48
5		NSD001	Nose Disease	51
6		NSN001	Nose, Anomalous Shape of	10
7		OLF004	Olfactory Nerve Neoplasm	22
8		HRY006	Hairy Nose Tip	14
9		BFD005	Bifid Nose, Autosomal Recessive	9
10		EVN003	Even-Plus Syndrome	25
11	P	RHN004	Rhinitis	62
12	c	CHR048	Chronic Rhinitis	41
13		BSM002	Bosma Arhinia Microphthalmia Syndrome	35
14		OLF002	Olfactory Groove Meningioma	27
15		PRM135	Paramedian Nasal Cleft	11
16		NSL005	Nasal Cavity Olfactory Neuroblastoma	6
17		OLF003	Olfactory Neural Tumor	5
18		HYD018	Hydrocephalus Craniosynostosis Bifid Nose	2
19		ATM008	Autoimmune Disease of Eyes, Ear, Nose and Throat	5
20		TNG004	Tongue Disease	37
21		PRB002	Proboscis Lateralis	14
22		ISL111	Isolated Arrhinia	13
23		BFD004	Bifid Nose, Autosomal Dominant	9
24		PLY086	Polyrrhinia	6
25		CHN065	Choanal Atresia, Posterior	43
26		SLN006	Silent Sinus Syndrome	20
27		SPR065	Supernumerary Nostril	19
28		NSL017	Nasolacrimal Duct Cyst	15
29		CRN192	Craniorhiny	14
30		NSL020	Nasal Glial Heterotopia	14
31		NSL021	Nasal Encephalocele	12
32		CHN052	Choanal Atresia, Bilateral	6
33		INT285	Intractable Diarrhea-Choanal Atresia-Eye Anomalies Syndrome	5
34		CHN051	Choanal Atresia, Unilateral	5
35		CNG227	Congenital Nasal Pyriform Aperture Stenosis with Holoprosencephaly	5
36		SPR109	Supratip Dysplasia	4
37		HYP737	Hyperhidrosis, Gustatory	36
38		OLF001	Olfactory Nerve Disease	18
39	c	ZMM002	Zimmermann-Laband Syndrome 1	38
40	P	ZMM001	Zimmermann-Laband Syndrome	28
41	c	ZMM003	Zimmermann-Laband Syndrome 2	18
42		ARR002	Arrhinia	11
43		SPN248	Spondyloepimetaphyseal Dysplasia, Sponastrime Type	31
44		WLF002	Wolf-Hirschhorn Syndrome	54
45		MRS002	Marshall Syndrome	45
46		HYP513	Hypogonadotropic Hypogonadism 1 with or Without Anosmia	40
47		RPD002	Rapadilino Syndrome	39
48		HRN021	Hernández-Aguirre Negrete Syndrome	14
49		VLJ001	Viljoen Kallis Voges Syndrome	10
50		ARH001	Arhinia Choanal Atresia Microphthalmia	9
51	P	KLL001	Kallmann Syndrome	63
52	c	RBN021	Rubinstein-Taybi Syndrome 1	50
53	c	RBN008	Rubinstein-Taybi Syndrome 2	25
54		DWR018	Dwarfism, Levi Type	13
55	c	KLL005	Kallmann Syndrome 3	9
56	c	KLL007	Kallmann Syndrome 5	9
57	c	KLL006	Kallmann Syndrome 4	9
58	c	KLL008	Kallmann Syndrome 6	8
59		CRM008	Crumpled Helices and Small Mouth	7
60	P	RBN007	Rubinstein Taybi Like Syndrome	6
61		MLN017	Milner Khallouf Gibson Syndrome	5
62		LCR013	Lacrimal Duct Defect	31
63		BLP009	Blepharonasofacial Malformation Syndrome	20
64		ANS017	Anosmia, Isolated Congenital	19
65		CHN040	Choanal Atresia and Lymphedema	19
66		RDL029	Radial Ray Hypoplasia with Choanal Atresia	16
67		RNS001	Raine Syndrome	45
68		FLT006	Floating-Harbor Syndrome	45
69		CRN048	Craniofacial-Deafness-Hand Syndrome	29
70		JNS005	Jones Hersh Yusk Syndrome	10
71		LCR014	Lacrimoauriculodentodigital Syndrome	59
72		FML079	Familial Nasal Acilia	11