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 57

Characteristics:

OMIM:

57
Inheritance:
autosomal dominant


HPO:

32
androstenone, ability to smell:
Inheritance autosomal dominant inheritance


External Ids:

OMIM 57 105570
MedGen 42 C1862934
SNOMED-CT via HPO 69 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

Symptoms via clinical synopsis from OMIM:

57
Neuro:
ability to smell androstenone


Clinical features from OMIM:

105570

Human phenotypes related to Androstenone, Ability to Smell:

32
# Description HPO Frequency HPO Source Accession
1 abnormality of the nervous system 32 HP:0000707

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 ExPASy
19 FMA
28 GO
29 GTR
30 HGMD
31 HMDB
32 HPO
33 ICD10
34 ICD10 via Orphanet
35 ICD9CM
36 IUPHAR
37 KEGG
38 LifeMap
40 LOVD
42 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
54 NINDS
55 Novoseek
57 OMIM
58 OMIM via Orphanet
62 PubMed
64 QIAGEN
69 SNOMED-CT via HPO
70 SNOMED-CT via Orphanet
71 TGDB
72 Tocris
73 UMLS
74 UMLS via Orphanet
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