Abnormality of the sense of smell

Symptom Information:

Symptom ID: HPO:0004408
Abnormality of olfaction [HPO:0004408]
Smell defect [HPO:0004408]
Olfaction anomaly [Orphanet:8000]
Smell defect [OMIM:Smell defect]
Anomalies of nose and olfaction [Orphanet:8000]
Cross references:
Orphanet:8000 "Anomalies of nose and olfaction" [Orphanet:8000]
OMIM: "Smell defect" [OMIM:Smell defect]
Is a (Direct Parents):
HPO         Abnormal peripheral nervous system morphology
Orphanet Abnormality of the nose
HPO         Abnormality of the nose
Is a (Whole tree): HPO:
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system morphology(HPO:0012639)
             Abnormal peripheral nervous system morphology(HPO:0000759)
                Abnormality of the sense of smell(HPO:0004408)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the face(HPO:0000271)
                Abnormality of the nose(HPO:0000366)
                   Abnormality of the sense of smell(HPO:0004408)
Database Frequency: 28 / 7739

All diseases associated with this symptom:

8p11.2 deletion syndrome (Orphanet:251066)
Absent thumb - short stature - immunodeficiency (Orphanet:2951)
Acro-renal-mandibular syndrome (Orphanet:958)
Aniridia (Orphanet:77)
Arrhinia (Orphanet:1134)
Arrhinia - choanal atresia - microphthalmia (Orphanet:1135)
Blepharophimosis - ptosis - esotropia - syndactyly - short stature (Orphanet:2057)
Bloom syndrome (Orphanet:125)
Brachytelephalangy - dysmorphism - Kallmann syndrome (Orphanet:1295)
CHARGE syndrome (Orphanet:138)
Campomelic dysplasia (Orphanet:140)
Cronkhite-Canada syndrome (Orphanet:2930)
Fronto-facio-nasal dysostosis (Orphanet:1791)
Gorlin syndrome (Orphanet:377)
Hartsfield-Bixler-Demyer syndrome (Orphanet:2117)
Holoprosencephaly (Orphanet:2162)
Hyposmia - nasal and ocular hypoplasia - hypogonadotropic hypogonadism (Orphanet:2250)
Kallmann syndrome (Orphanet:478)
Kallmann syndrome - heart disease (Orphanet:2326)
Leber congenital amaurosis 10 (OMIM:611755)
Moebius syndrome (Orphanet:570)
Neuroectodermal syndrome, Johnson type (Orphanet:2316)
Refsum disease (Orphanet:773)
Septo-optic dysplasia (Orphanet:3157)
Syndromic X-linked ichthyosis (Orphanet:281090)
Tetraamelia - multiple malformations (Orphanet:3301)
Wolfram syndrome 1 (OMIM:222300)