MCID: AND018
MIFTS: 6

Androstenone, Ability to Smell

Aliases & Classifications for Androstenone, Ability to Smell

MalaCards integrated aliases for Androstenone, Ability to Smell:

Name: Androstenone, Ability to Smell 58

Characteristics:

OMIM:

58
Inheritance:
autosomal dominant


HPO:

33
androstenone, ability to smell:
Inheritance autosomal dominant inheritance


External Ids:

OMIM 58 105570
MedGen 43 C1862934
SNOMED-CT via HPO 70 263681008 88425004

Summaries for Androstenone, Ability to Smell

MalaCards based summary : Androstenone, Ability to Smell Related phenotype is abnormality of the nervous system.

Description from OMIM: 105570

Related Diseases for Androstenone, Ability to Smell

Symptoms & Phenotypes for Androstenone, Ability to Smell

Human phenotypes related to Androstenone, Ability to Smell:

33
# Description HPO Frequency HPO Source Accession
1 abnormality of the nervous system 33 HP:0000707

Symptoms via clinical synopsis from OMIM:

58
Neuro:
ability to smell androstenone

Clinical features from OMIM:

105570

Drugs & Therapeutics for Androstenone, Ability to Smell

Search Clinical Trials , NIH Clinical Center for Androstenone, Ability to Smell

Genetic Tests for Androstenone, Ability to Smell

Anatomical Context for Androstenone, Ability to Smell

Publications for Androstenone, Ability to Smell

Variations for Androstenone, Ability to Smell

Expression for Androstenone, Ability to Smell

Search GEO for disease gene expression data for Androstenone, Ability to Smell.

Pathways for Androstenone, Ability to Smell

GO Terms for Androstenone, Ability to Smell

Sources for Androstenone, Ability to Smell

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
20 FMA
29 GO
30 GTR
31 HGMD
32 HMDB
33 HPO
34 ICD10
35 ICD10 via Orphanet
36 ICD9CM
37 IUPHAR
38 KEGG
39 LifeMap
41 LOVD
43 MedGen
45 MeSH
46 MESH via Orphanet
47 MGI
50 NCI
51 NCIt
52 NDF-RT
55 NINDS
56 Novoseek
58 OMIM
59 OMIM via Orphanet
63 PubMed
65 QIAGEN
70 SNOMED-CT via HPO
71 SNOMED-CT via Orphanet
72 TGDB
73 Tocris
74 UMLS
75 UMLS via Orphanet
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