Anosmia
Symptom Information:
Symptom ID: | HPO:0000458 | |||||||||||||||||
Synonyms: |
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Quality: | ||||||||||||||||||
Cross references: |
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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 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) 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) MedDRA: Nervous system disorders(MedDRA:10029205) Cranial nerve disorders (excl neoplasms)(MedDRA:10011305) Olfactory nerve disorders(MedDRA:10030281) Anosmia(HPO:0000458) |
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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) |