# |
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 |