Hyposmia

Symptom Information:

Symptom ID: HPO:0004409
Synonyms:
Decreased smell sensation [HPO:0004409]
Sense of smell impaired [HPO:0004409]
Sense of smell impaired (finding) [Orphanet:8810]
Sense of smell impaired [Orphanet:8810]
Decreased smell sensation [OMIM:Decreased smell sensation]
Hyposmia [OMIM:Hyposmia]
Anosmia/cacosmia/hypogeusia/hyposmia/olfactory bulb hypoplasia [Orphanet:8810]
Hyposmia [Orphanet:8810]
Hyposmia [MedDRA:10050515]
Diminished sense of smell [MedDRA:10050515]
Olfactory bulb hypoplasia [Orphanet:8810]
Hypogeusia [MedDRA:10020989]
Hypogeusia [Orphanet:8810]
Cacosmia [MedDRA:10049878]
Dysosmia [Orphanet:8810]
Quality:
Cross references:
Orphanet:8810 "Anosmia/cacosmia/hypogeusia/hyposmia/olfactory bulb hypoplasia" [Orphanet:8810]
OMIM: "Decreased smell sensation" [OMIM:Decreased smell sensation]
OMIM: "Hyposmia" [OMIM:Hyposmia]
UMLS:C0234260 "Hyposmia" [HPO:0004409]
UMLS:C0234260 "Sense of smell impaired" [Orphanet:8810]
UMLS:C0151934 "Hypogeusia" [Orphanet:8810]
UMLS:C0235287 "Dysosmia" [Orphanet:8810]
Is a (Direct Parents):
HPO         Abnormality of the sense of smell
Orphanet Anosmia
Orphanet Abnormality of the nose
MedDRA Olfactory nerve disorders
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       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)
                      Hyposmia(HPO:0004409)
       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)
                   Hyposmia(HPO:0004409)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Cranial nerve disorders (excl neoplasms)(MedDRA:10011305)
       Olfactory nerve disorders(MedDRA:10030281)
          Hyposmia(HPO:0004409)
Database Frequency: 16 / 7739
Resource:

All diseases associated with this symptom:

AURAL ATRESIA, CONGENITAL (OMIM:607842)
Arrhinia - choanal atresia - microphthalmia (Orphanet:1135)
Bardet-Biedl syndrome 17 (OMIM:615994)
Bardet-Biedl syndrome 19 (OMIM:615996)
Bardet-Biedl syndrome 5 (OMIM:615983)
Channelopathy-associated congenital insensitivity to pain (Orphanet:88642)
Friedreich ataxia 1 (OMIM:229300)
Kufor-Rakeb syndrome (Orphanet:306674)
LEOPARD SYNDROME 1 (OMIM:151100)
Leber congenital amaurosis 10 (OMIM:611755)
Leukoencephalopathy - dystonia - motor neuropathy (Orphanet:163684)
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, ADULT-ONSET, WITH ANOSMIA (OMIM:608720)
Noonan syndrome with multiple lentigines (Orphanet:500)
PARKINSON DISEASE 8, AUTOSOMAL DOMINANT (OMIM:607060)
Parkinsonim due to ATP13A2 deficiency (Orphanet:314632)
Wolfram syndrome 1 (OMIM:222300)