Hyposmia
Symptom Information:
Symptom ID: | HPO:0004409 | |||||||||||||||
Synonyms: |
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Is a (Direct Parents): |
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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) Hyposmia(HPO:0004409) 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) MedDRA: Nervous system disorders(MedDRA:10029205) Cranial nerve disorders (excl neoplasms)(MedDRA:10011305) Olfactory nerve disorders(MedDRA:10030281) Hyposmia(HPO:0004409) |
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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) |