molecular messenger
CHEBI:CHEBI_33280
Alternative Names
- chemical messenger
Treatment Applications
-
cone-rod dystrophy 5View Disease →
DOID:0111010
-
cone-rod dystrophy 7View Disease →
DOID:0111012
-
cone-rod dystrophy 3View Disease →
DOID:0111013
-
cone-rod dystrophy 17View Disease →
DOID:0111023
-
myostatin-related muscle hypertrophyView Disease →
DOID:0111072
-
autosomal recessive hyaline body myopathyView Disease →
DOID:0111268
-
solitary median maxillary central incisorView Disease →
DOID:0111380
-
trichohepatoenteric syndrome 1View Disease →
DOID:0111415
-
familial isolated trichomegalyView Disease →
DOID:0111566
-
X-linked deafness 4View Disease →
DOID:0111735
-
X-linked deafness 7View Disease →
DOID:0111738
-
X-linked deafness 6View Disease →
DOID:0111740
-
Y-linked deafness 1View Disease →
DOID:0111759
-
frontometaphyseal dysplasia 1View Disease →
DOID:0111786
-
syndromic microphthalmia 14View Disease →
DOID:0111802
-
syndromic microphthalmia 11View Disease →
DOID:0111804
-
syndromic microphthalmia 13View Disease →
DOID:0111811
-
Meester-Loeys syndromeView Disease →
DOID:0111861
-
spermatogenic failure 41View Disease →
DOID:0111912
-
spermatogenic failure 43View Disease →
DOID:0111917
-
spermatogenic failure 38View Disease →
DOID:0111919
-
spermatogenic failure 29View Disease →
DOID:0111930
-
spermatogenic failure 44View Disease →
DOID:0112109
-
spermatogenic failure 45View Disease →
DOID:0112163
-
spermatogenic failure 46View Disease →
DOID:0112164
-
spermatogenic failure 47View Disease →
DOID:0112175
-
spermatogenic failure 48View Disease →
DOID:0112176
-
mismatch repair cancer syndromeView Disease →
DOID:0112182
-
lissencephaly 7 with cerebellar hypoplasiaView Disease →
DOID:0112231
-
pontocerebellar hypoplasia type 14View Disease →
DOID:0112325
-
pontocerebellar hypoplasia type 15View Disease →
DOID:0112326
-
spermatogenic failure 55View Disease →
DOID:0112337
-
hereditary spastic paraplegia 86View Disease →
DOID:0112342
-
hereditary spastic paraplegia 81View Disease →
DOID:0112349
-
spermatogenic failure 64View Disease →
DOID:0112353
-
Arts syndromeView Disease →
DOID:0050647
-
Armfield syndromeView Disease →
DOID:0050764
-
permanent neonatal diabetes mellitusView Disease →
DOID:0060639
-
Coffin-Siris syndrome 2View Disease →
DOID:0070044
-
GAND syndromeView Disease →
DOID:0070048
-
spermatogenic failure 19View Disease →
DOID:0070170
-
familial partial lipodystrophy type 5View Disease →
DOID:0070203
-
familial partial lipodystrophy type 1View Disease →
DOID:0070207
-
hereditary lymphedema IDView Disease →
DOID:0070209
-
hereditary lymphedema IAView Disease →
DOID:0070210
-
primary autosomal recessive microcephaly 6View Disease →
DOID:0070290
-
primary autosomal dominant microcephaly 18View Disease →
DOID:0070295
-
hereditary spastic paraplegia 70View Disease →
DOID:0070454
-
age related macular degeneration 5View Disease →
DOID:0110028
-
Bartter disease type 5View Disease →
DOID:0110147
-
Charcot-Marie-Tooth disease type 4DView Disease →
DOID:0110186
-
hypertrophic cardiomyopathy 21View Disease →
DOID:0110311
-
retinitis pigmentosa 46View Disease →
DOID:0110409
-
long QT syndrome 14View Disease →
DOID:0110655
-
long QT syndrome 15View Disease →
DOID:0110656
-
hereditary spastic paraplegia 14View Disease →
DOID:0110767
-
hereditary spastic paraplegia 16View Disease →
DOID:0110769
-
hereditary spastic paraplegia 23View Disease →
DOID:0110774
-
hereditary spastic paraplegia 24View Disease →
DOID:0110775
-
hereditary spastic paraplegia 25View Disease →
DOID:0110776
-
hereditary spastic paraplegia 26View Disease →
DOID:0110777
-
hereditary spastic paraplegia 27View Disease →
DOID:0110778
-
hereditary spastic paraplegia 28View Disease →
DOID:0110779
-
hereditary spastic paraplegia 33View Disease →
DOID:0110784
-
hereditary spastic paraplegia 36View Disease →
DOID:0110787
-
hereditary spastic paraplegia 37View Disease →
DOID:0110788
-
hereditary spastic paraplegia 38View Disease →
DOID:0110789
-
hereditary spastic paraplegia 41View Disease →
DOID:0110793
-
hereditary spastic paraplegia 42View Disease →
DOID:0110794
-
hereditary spastic paraplegia 43View Disease →
DOID:0110795
-
hereditary spastic paraplegia 44View Disease →
DOID:0110796
-
hereditary spastic paraplegia 45View Disease →
DOID:0110797
-
hereditary spastic paraplegia 46View Disease →
DOID:0110798
-
hereditary spastic paraplegia 47View Disease →
DOID:0110799
-
hereditary spastic paraplegia 48View Disease →
DOID:0110800
-
hereditary spastic paraplegia 53View Disease →
DOID:0110805
-
hereditary spastic paraplegia 55View Disease →
DOID:0110807
-
hereditary spastic paraplegia 56View Disease →
DOID:0110808
-
hereditary spastic paraplegia 5AView Disease →
DOID:0110810
-
hereditary spastic paraplegia 6View Disease →
DOID:0110811
-
hereditary spastic paraplegia 61View Disease →
DOID:0110812
-
hereditary spastic paraplegia 62View Disease →
DOID:0110813
-
hereditary spastic paraplegia 74View Disease →
DOID:0110819
-
hereditary spastic paraplegia 75View Disease →
DOID:0110820
-
hereditary spastic paraplegia 8View Disease →
DOID:0110823
-
Usher syndrome type 1View Disease →
DOID:0110826
-
Usher syndrome type 3AView Disease →
DOID:0110841
-
Waardenburg syndrome type 1View Disease →
DOID:0110948
-
Waardenburg syndrome type 2AView Disease →
DOID:0110950
-
Waardenburg syndrome type 4AView Disease →
DOID:0110953
-
Joubert syndrome 21View Disease →
DOID:0110990
-
Joubert syndrome 22View Disease →
DOID:0110991
-
Joubert syndrome 23View Disease →
DOID:0110992
-
Joubert syndrome 24View Disease →
DOID:0110993
-
Joubert syndrome 5View Disease →
DOID:0111000
Drug Classification
-
biological roleView Class →
CHEBI:24432
-
semiochemicalView Class →
CHEBI:26645
-
hormoneView Class →
CHEBI:24621
-
signalling moleculeView Class →
CHEBI:62488
-
neurotransmitterView Class →
CHEBI:25512
Important Medical Information
⚕️ This information is sourced from ChEBI (Chemical Entities of Biological Interest) database and is intended for educational purposes only.
- Always consult with a healthcare professional before starting, stopping, or modifying any medication.
- Side effects may vary and this list may not be comprehensive.
- Drug interactions may occur with other medications.
Additional Identifiers
- core#notation
- CHEBI:33280
🔍 Click on any linked disease name to learn more about the conditions this medication is used to treat, or explore related drug classifications for more information about similar medications.
Additional Attributes
- oboInOwl#hasOBONamespace
- chebi_ontology
- oboInOwl#id
- CHEBI:33280
- core#notation
- CHEBI:33280
- oboInOwl#inSubset
- http://purl.obolibrary.org/obo/chebi#3_STAR
- 22-rdf-syntax-ns#type
- http://www.w3.org/2002/07/owl#Class
- rdf-schema#range
- https://w3id.org/def/predibionto#has_drug_105328
- RO_0000087
- http://purl.obolibrary.org/obo/CHEBI_25375
- owl#someValuesFrom
- t152172
- owl#annotatedSource
- t190579