Anosmia

Symptom Information:

Symptom ID: HPO:0000458
Synonyms:
Loss of sense of smell [HPO:0000458]
Loss of sense of smell (finding) [Orphanet:8810]
Anosmia [Orphanet:8810]
Anosmia [OMIM:Anosmia]
Anosmia/cacosmia/hypogeusia/hyposmia/olfactory bulb hypoplasia [Orphanet:8810]
Anosmia [MedDRA:10002653]
Loss of smell [MedDRA:10002653]
Smell loss [MedDRA:10002653]
Anosmia (1 patient) [OMIM:Anosmia (1 patient)]
Anosmia (in contiguous gene syndrome patients) [OMIM:Anosmia (in contiguous gene syndrome patients)]
Anosmia (in some patients) [OMIM:Anosmia (in some patients)]
Anosmia (rare) [OMIM:Anosmia (rare)]
Olfactory bulb hypoplasia [Orphanet:8810]
Hypogeusia [MedDRA:10020989]
Hypogeusia [Orphanet:8810]
Cacosmia [MedDRA:10049878]
Dysosmia [Orphanet:8810]
Quality:
Cross references:
HPO:0010632 "Total anosmia" [Orphanet:8810]
Orphanet:8810 "Anosmia/cacosmia/hypogeusia/hyposmia/olfactory bulb hypoplasia" [Orphanet:8810]
OMIM: "Anosmia" [OMIM:Anosmia]
OMIM: "Anosmia (1 patient)" [OMIM:Anosmia (1 patient)]
OMIM: "Anosmia (in contiguous gene syndrome patients)" [OMIM:Anosmia (in contiguous gene syndrome patients)]
OMIM: "Anosmia (in some patients)" [OMIM:Anosmia (in some patients)]
OMIM: "Anosmia (rare)" [OMIM:Anosmia (rare)]
UMLS:C0003126 "Anosmia" [HPO:0000458]
UMLS:C0003126 "Anosmia" [Orphanet:8810]
UMLS:C0151934 "Hypogeusia" [Orphanet:8810]
UMLS:C0235287 "Dysosmia" [Orphanet:8810]
Is a (Direct Parents):
MedDRA Olfactory nerve disorders
Orphanet Abnormality of the nose
HPO         Abnormality of the sense of smell
Is a (Whole tree): HPO:
All(HPO:0000001)
    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)
                   Anosmia(HPO:0000458)
       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)
                      Anosmia(HPO:0000458)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Cranial nerve disorders (excl neoplasms)(MedDRA:10011305)
       Olfactory nerve disorders(MedDRA:10030281)
          Anosmia(HPO:0000458)
Database Frequency: 49 / 7739
Resource:

All diseases associated with this symptom:

AL amyloidosis (Orphanet:85443)
ANOSMIA (OMIM:301700)
APNEA, OBSTRUCTIVE SLEEP (OMIM:107650)
Absent thumb - short stature - immunodeficiency (Orphanet:2951)
Bardet-Biedl syndrome 13 (OMIM:615990)
Bardet-Biedl syndrome 4 (OMIM:615982)
Blepharophimosis - ptosis - esotropia - syndactyly - short stature (Orphanet:2057)
Brachytelephalangic chondrodysplasia punctata (Orphanet:79345)
Brachytelephalangy - dysmorphism - Kallmann syndrome (Orphanet:1295)
CHARGE syndrome (Orphanet:138)
CHONDRODYSPLASIA PUNCTATA 1, X-LINKED RECESSIVE (OMIM:302950)
CILIARY DYSKINESIA, PRIMARY, 1 (OMIM:244400)
Channelopathy-associated congenital insensitivity to pain (Orphanet:88642)
HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA (OMIM:308700)
HYPOGONADOTROPIC HYPOGONADISM 10 WITH OR WITHOUT ANOSMIA (OMIM:614839)
HYPOGONADOTROPIC HYPOGONADISM 12 WITH OR WITHOUT ANOSMIA (OMIM:614841)
HYPOGONADOTROPIC HYPOGONADISM 13 WITH OR WITHOUT ANOSMIA (OMIM:614842)
HYPOGONADOTROPIC HYPOGONADISM 14 WITH OR WITHOUT ANOSMIA (OMIM:614858)
HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA (OMIM:614897)
HYPOGONADOTROPIC HYPOGONADISM 18 WITH OR WITHOUT ANOSMIA (OMIM:615267)
HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA (OMIM:147950)
HYPOGONADOTROPIC HYPOGONADISM 22 WITH OR WITHOUT ANOSMIA (OMIM:616030)
HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA (OMIM:244200)
HYPOGONADOTROPIC HYPOGONADISM 4 WITH OR WITHOUT ANOSMIA (OMIM:610628)
HYPOGONADOTROPIC HYPOGONADISM 5 WITH OR WITHOUT ANOSMIA (OMIM:612370)
HYPOGONADOTROPIC HYPOGONADISM 6 WITH OR WITHOUT ANOSMIA (OMIM:612702)
HYPOGONADOTROPIC HYPOGONADISM 8 WITH OR WITHOUT ANOSMIA (OMIM:614837)
HYPOGONADOTROPIC HYPOGONADISM 9 WITH OR WITHOUT ANOSMIA (OMIM:614838)
Hereditary motor and sensory neuropathy type 6 (Orphanet:90120)
ICHTHYOSIS AND MALE HYPOGONADISMRUD SYNDROME, INCLUDED (OMIM:308200)
ISOVALERIC ACID, INABILITY TO SMELL (OMIM:243450)
Isolated congenital anosmia (Orphanet:88620)
KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA (OMIM:308750)
Kallmann syndrome (Orphanet:478)
Kufor-Rakeb syndrome (Orphanet:306674)
MUSK, INABILITY TO SMELL (OMIM:254150)
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, ADULT-ONSET, WITH ANOSMIA (OMIM:608720)
Nasal dermoid cyst (Orphanet:141103)
Neuroectodermal syndrome, Johnson type (Orphanet:2316)
Neurologic Waardenburg-Shah syndrome (Orphanet:163746)
Parkinsonim due to ATP13A2 deficiency (Orphanet:314632)
Primary localized amyloidosis (Orphanet:314709)
REFSUM DISEASE, CLASSIC (OMIM:266500)
Refsum disease (Orphanet:773)
SKUNK N-BUTYLMERCAPTAN, INABILITY TO SMELL (OMIM:270350)
Solitary median maxillary central incisor syndrome (Orphanet:2286)
WAARDENBURG SYNDROME, TYPE 2E (OMIM:611584)
WAARDENBURG SYNDROME, TYPE 4C (OMIM:613266)
Wolfram syndrome 1 (OMIM:222300)