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Egenskap
Enlarged male breast
Klinisk navn: Gynecomastia
Abnormal development of large mammary glands in males resulting in breast enlargement.
Sammendrag
- Også kalt
- Gynaecomastia
- Kroppssystem
- Abnormality of the breast
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Denne siden som data
Legg til .json etter adressen til siden, eller be om application/json, for å lese den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/gynecomastia.json"
page <- fromJSON(url)
page$trait$nameEnlarged male breastHP:0000771
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Les genene knyttet til Enlarged male breast, og resten av genomet ditt, med én test.
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Få mitt Genome Test73 condition reports read genes linked to this trait
Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Hypogonadotropic HypogonadismReads 26 of these genesLEPLEPRNR0B1RBM28RNF216CHD7About this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 10 of these genesARCYP11A1DHX37GATA4MAP3K1NR5A1About this report →
- Congenital Adrenal HyperplasiaReads 5 of these genesCYP11A1CYP17A1HSD3B2CYP11B1CYP21A2About this report →
- 46,XX Differences of Sex DevelopmentReads 3 of these genesNR5A1SRYRSPO1About this report →
Show 69 more reports
- Carney Complex & Hereditary Adrenal Cushing SyndromeReads 2 of these genesPDE11APRKAR1AAbout this report →
- Androgen Insensitivity SyndromeReads 1 of these genesARAbout this report →
- Campomelic DysplasiaReads 1 of these genesSOX9About this report →
- CHARGE SyndromeReads 1 of these genesCHD7About this report →
- DCC-Related Mirror Movements and Agenesis of the Corpus CallosumReads 1 of these genesDCCAbout this report →
- Dias-Logan SyndromeReads 1 of these genesBCL11AAbout this report →
- Fragile X SyndromeReads 1 of these genesFMR1About this report →
- Frank-Ter Haar SyndromeReads 1 of these genesSH3PXD2BAbout this report →
- H SyndromeReads 1 of these genesSLC29A3About this report →
- Peutz-Jeghers SyndromeReads 1 of these genesSTK11About this report →
- PNPLA6-Related Ataxia, Retinal Dystrophy and HypogonadismReads 1 of these genesPNPLA6About this report →
- POLR3A-Related DisorderReads 1 of these genesPOLR3AAbout this report →
- Primrose SyndromeReads 1 of these genesZBTB20About this report →
- Rett Syndrome and MECP2-Related DisordersReads 1 of these genesMECP2About this report →
- SCN4A-Related Congenital MyopathyReads 1 of these genesSCN4AAbout this report →
- Spinal and Bulbar Muscular Atrophy (Kennedy Disease)Reads 1 of these genesARAbout this report →
- SPTBN1-Related Neurodevelopmental DisorderReads 1 of these genesSPTBN1About this report →
- TCF20-Related Neurodevelopmental DisorderReads 1 of these genesTCF20About this report →
- Monogenic Obesity (Leptin-Melanocortin Pathway)Reads 2 of these genesLEPLEPRAbout this report →
- Cowden Syndrome (PTEN hamartoma tumour syndrome)Reads 1 of these genesPTENAbout this report →
- Familial Isolated Pituitary Adenoma (FIPA / X-LAG)Reads 1 of these genesAIPAbout this report →
- Hereditary Wilms TumourReads 1 of these genesWT1About this report →
- Severe Inherited Insulin ResistanceReads 1 of these genesAKT2About this report →
- Hypertrophic CardiomyopathyReads 5 of these genesDHX37MAP3K1NR5A1SRYZFPM2About this report →
- LipodystrophyReads 2 of these genesPLAAT3AKT2About this report →
- Congenital Diaphragmatic Hernia (Monogenic)Reads 1 of these genesZFPM2About this report →
- Familial Periodic ParalysisReads 1 of these genesSCN4AAbout this report →
- Tetralogy of FallotReads 1 of these genesZFPM2About this report →
- Diabetes MellitusReads 3 of these genesAKT2GATA4ZBTB20About this report →
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 1 of these genesPRKAR1AAbout this report →
- Hereditary Methaemoglobinaemia and Unstable HaemoglobinsReads 1 of these genesCYB5AAbout this report →
- Mosaic Variegated Aneuploidy SyndromeReads 1 of these genesSMC5About this report →
- MTOR Pathway Megalencephaly and Overgrowth DisordersReads 1 of these genesPIK3CAAbout this report →
- Female InfertilityReads 3 of these genesCYP19A1NR5A1FMR1About this report →
- Cornelia de Lange SyndromeReads 1 of these genesHDAC8About this report →
- HemochromatosisReads 1 of these genesHFEAbout this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 2 of these genesRBM28HESX1About this report →
- Waardenburg SyndromeReads 1 of these genesSOX10About this report →
- Inherited Neurodegenerative DisordersReads 7 of these genesARPNPLA6RNF216WWOXFMR1POLR3AAbout this report →
- Familial Glucocorticoid DeficiencyReads 1 of these genesNR0B1About this report →
- Malignant Endocrine NeoplasmReads 1 of these genesMEN1About this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesDESAbout this report →
- Intellectual DisabilityReads 5 of these genesLAS1LPHF6CUL4BWDR11MECP2About this report →
- Arrhythmogenic CardiomyopathyReads 1 of these genesDESAbout this report →
- Usher SyndromeReads 1 of these genesCDH23About this report →
- Type I InterferonopathiesReads 1 of these genesPSMB8About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesGATA4About this report →
- Myofibrillar MyopathiesReads 1 of these genesDESAbout this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 2 of these genesWWOXCOQ8AAbout this report →
- Monogenic Hypertension & Mineralocorticoid DisordersReads 1 of these genesCYP11B1About this report →
- Epidermolysis BullosaReads 1 of these genesITGA3About this report →
- Neonatal Diabetes MellitusReads 1 of these genesGATA4About this report →
- Bardet-Biedl and Alström SyndromesReads 1 of these genesALMS1About this report →
- Syndromic CraniosynostosisReads 1 of these genesFGFR1About this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 1 of these genesPOLR3AAbout this report →
- Congenital Myasthenic SyndromeReads 1 of these genesSCN4AAbout this report →
- Thyroid CancerReads 1 of these genesMEN1About this report →
- Osteogenesis ImperfectaReads 1 of these genesPOLR3AAbout this report →
- Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesPSMB8About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 1 of these genesRSPO1About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesSCN4AAbout this report →
- Epilepsy (Full Panel)Reads 2 of these genesWWOXMECP2About this report →
- Dilated CardiomyopathyReads 1 of these genesDESAbout this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesPNPLA6About this report →
- Other Inherited LeukodystrophiesReads 1 of these genesPOLR3AAbout this report →
- Hearing Loss and DeafnessReads 1 of these genesCDH23About this report →
- Primary Mitochondrial DiseaseReads 1 of these genesCOQ8AAbout this report →
- Other Inborn Errors of ImmunityReads 1 of these genesRELAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 1 of these genesCOQ8AAbout this report →
Les genene knyttet til Enlarged male breast, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test99 gener knyttet til Enlarged male breast
Endringer i disse genene forårsaker sjeldne tilstander der Enlarged male breast forekommer. De fleste med denne egenskapen har ingen av disse tilstandene, og et gen på denne listen sier ingenting om noens eget genom.
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| PLAAT3phospholipase A and acyltransferase 3 | Alltid | I 1 tilstand |
| RFC4replication factor C subunit 4 | Alltid | I 1 tilstand |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Alltid | I 1 tilstand |
| AKT2AKT serine/threonine kinase 2 | Svært ofte (80–99 %) | I 2 tilstander |
| ARandrogen receptor | Svært ofte (80–99 %) | I 5 tilstander |
| CYP11A1cytochrome P450 family 11 subfamily A member 1 | Svært ofte (80–99 %) | I 2 tilstander |
| CYP19A1cytochrome P450 family 19 subfamily A member 1 | Svært ofte (80–99 %) | I 1 tilstand |
| DHX37DEAH-box helicase 37 | Svært ofte (80–99 %) | I 1 tilstand |
| GATA4GATA binding protein 4 | Svært ofte (80–99 %) | I 1 tilstand |
| HDAC8histone deacetylase 8 | Svært ofte (80–99 %) | I 1 tilstand |
| LAS1LLAS1 like ribosome biogenesis factor | Svært ofte (80–99 %) | I 2 tilstander |
| LEPleptin | Svært ofte (80–99 %) | I 2 tilstander |
| LEPRleptin receptor | Svært ofte (80–99 %) | I 1 tilstand |
| MAP3K1mitogen-activated protein kinase kinase kinase 1 | Svært ofte (80–99 %) | I 1 tilstand |
| NR0B1nuclear receptor subfamily 0 group B member 1 | Svært ofte (80–99 %) | I 1 tilstand |
| NR5A1nuclear receptor subfamily 5 group A member 1 | Svært ofte (80–99 %) | I 1 tilstand |
| PHF6PHD finger protein 6 | Svært ofte (80–99 %) | I 2 tilstander |
| PNPLA6patatin like domain 6, lysophospholipase | Svært ofte (80–99 %) | I 1 tilstand |
| RBM28RNA binding motif protein 28 | Svært ofte (80–99 %) | I 2 tilstander |
| RNF216ring finger protein 216 | Svært ofte (80–99 %) | I 1 tilstand |
| SOX9SRY-box transcription factor 9 | Svært ofte (80–99 %) | I 1 tilstand |
| SRYsex determining region Y | Svært ofte (80–99 %) | I 3 tilstander |
| VAMP7vesicle associated membrane protein 7 | Svært ofte (80–99 %) | I 1 tilstand |
| WT1WT1 transcription factor | Svært ofte (80–99 %) | I 1 tilstand |
| WWOXWW domain containing oxidoreductase | Svært ofte (80–99 %) | I 1 tilstand |
| ZFPM2zinc finger protein, FOG family member 2 | Svært ofte (80–99 %) | I 1 tilstand |
| AIPAHR interacting HSP90 co-chaperone | Ofte (30–79 %) | I 1 tilstand |
| CDH23cadherin related 23 | Ofte (30–79 %) | I 2 tilstander |
| CHD7chromodomain helicase DNA binding protein 7 | Ofte (30–79 %) | I 2 tilstander |
| CPEcarboxypeptidase E | Ofte (30–79 %) | I 1 tilstand |
| CUL4Bcullin 4B | Ofte (30–79 %) | I 1 tilstand |
| CYP17A1cytochrome P450 family 17 subfamily A member 1 | Ofte (30–79 %) | I 3 tilstander |
| DESdesmin | Ofte (30–79 %) | I 1 tilstand |
| DUSP6dual specificity phosphatase 6 | Ofte (30–79 %) | I 2 tilstander |
| EMX2empty spiracles homeobox 2 | Ofte (30–79 %) | I 2 tilstander |
| FGF17fibroblast growth factor 17 | Ofte (30–79 %) | I 2 tilstander |
| FGF8fibroblast growth factor 8 | Ofte (30–79 %) | I 2 tilstander |
| FGFR1fibroblast growth factor receptor 1 | Ofte (30–79 %) | I 3 tilstander |
| FMR1fragile X messenger ribonucleoprotein 1 | Ofte (30–79 %) | I 1 tilstand |
| GNRH1gonadotropin releasing hormone 1 | Ofte (30–79 %) | I 1 tilstand |
Vis 59 gener til
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| GNRHRgonadotropin releasing hormone receptor | Ofte (30–79 %) | I 1 tilstand |
| HS6ST1heparan sulfate 6-O-sulfotransferase 1 | Ofte (30–79 %) | I 2 tilstander |
| HSD3B2hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2 | Ofte (30–79 %) | I 1 tilstand |
| KISS1KiSS-1 metastasis suppressor | Ofte (30–79 %) | I 1 tilstand |
| KISS1RKISS1 receptor | Ofte (30–79 %) | I 2 tilstander |
| LHBluteinizing hormone subunit beta | Ofte (30–79 %) | I 1 tilstand |
| MEN1menin 1 | Ofte (30–79 %) | I 1 tilstand |
| NHLH2nescient helix-loop-helix 2 | Ofte (30–79 %) | I 1 tilstand |
| NSMFNMDA receptor synaptonuclear signaling and neuronal migration factor | Ofte (30–79 %) | I 2 tilstander |
| PROK2prokineticin 2 | Ofte (30–79 %) | I 2 tilstander |
| PROKR2prokineticin receptor 2 | Ofte (30–79 %) | I 2 tilstander |
| SLC29A3solute carrier family 29 member 3 | Ofte (30–79 %) | I 2 tilstander |
| SMCHD1structural maintenance of chromosomes flexible hinge domain containing 1 | Ofte (30–79 %) | I 1 tilstand |
| SPRY4sprouty RTK signaling antagonist 4 | Ofte (30–79 %) | I 2 tilstander |
| TAC3tachykinin precursor 3 | Ofte (30–79 %) | I 1 tilstand |
| TACR3tachykinin receptor 3 | Ofte (30–79 %) | I 2 tilstander |
| TCF20transcription factor 20 | Ofte (30–79 %) | I 1 tilstand |
| TTI1TELO2 interacting protein 1 | Ofte (30–79 %) | I 1 tilstand |
| WDR11WD repeat domain 11 | Ofte (30–79 %) | I 2 tilstander |
| ZBTB20zinc finger and BTB domain containing 20 | Ofte (30–79 %) | I 2 tilstander |
| AFF4ALF transcription elongation factor 4 | Noen ganger (5–29 %) | I 1 tilstand |
| ALMS1ALMS1 centrosome and basal body associated protein | Noen ganger (5–29 %) | I 2 tilstander |
| ANOS1anosmin 1 | Noen ganger (5–29 %) | I 2 tilstander |
| BCL11ABCL11 transcription factor A | Noen ganger (5–29 %) | I 1 tilstand |
| BMP6bone morphogenetic protein 6 | Noen ganger (5–29 %) | I 1 tilstand |
| CCDC141coiled-coil domain containing 141 | Noen ganger (5–29 %) | I 1 tilstand |
| CYB5Acytochrome b5 type A | Noen ganger (5–29 %) | I 1 tilstand |
| CYP11B1cytochrome P450 family 11 subfamily B member 1 | Noen ganger (5–29 %) | I 1 tilstand |
| DCCDCC netrin 1 receptor | Noen ganger (5–29 %) | I 1 tilstand |
| ERMARDER membrane associated RNA degradation | Noen ganger (5–29 %) | I 1 tilstand |
| FEZF1FEZ family zinc finger 1 | Noen ganger (5–29 %) | I 1 tilstand |
| FLRT3fibronectin leucine rich transmembrane protein 3 | Noen ganger (5–29 %) | I 1 tilstand |
| HESX1HESX homeobox 1 | Noen ganger (5–29 %) | I 1 tilstand |
| HFEhomeostatic iron regulator | Noen ganger (5–29 %) | I 1 tilstand |
| HPGD15-hydroxyprostaglandin dehydrogenase | Noen ganger (5–29 %) | I 1 tilstand |
| HSD17B3hydroxysteroid 17-beta dehydrogenase 3 | Noen ganger (5–29 %) | I 2 tilstander |
| IL17RDinterleukin 17 receptor D | Noen ganger (5–29 %) | I 1 tilstand |
| MECP2methyl-CpG binding protein 2 | Noen ganger (5–29 %) | I 1 tilstand |
| NDNFneuron derived neurotrophic factor | Noen ganger (5–29 %) | I 1 tilstand |
| PDE11Aphosphodiesterase 11A | Noen ganger (5–29 %) | I 1 tilstand |
| POLR3ARNA polymerase III subunit A | Noen ganger (5–29 %) | I 2 tilstander |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Noen ganger (5–29 %) | I 1 tilstand |
| PSMB8proteasome 20S subunit beta 8 | Noen ganger (5–29 %) | I 1 tilstand |
| PTENphosphatase and tensin homolog | Noen ganger (5–29 %) | I 2 tilstander |
| RELREL proto-oncogene, NF-kB subunit | Noen ganger (5–29 %) | I 1 tilstand |
| SEMA3Asemaphorin 3A | Noen ganger (5–29 %) | I 1 tilstand |
| SH3PXD2BSH3 and PX domains 2B | Noen ganger (5–29 %) | I 1 tilstand |
| SLCO2A1solute carrier organic anion transporter family member 2A1 | Noen ganger (5–29 %) | I 1 tilstand |
| SMC5structural maintenance of chromosomes 5 | Noen ganger (5–29 %) | I 1 tilstand |
| SOX10SRY-box transcription factor 10 | Noen ganger (5–29 %) | I 1 tilstand |
| TMEM53transmembrane protein 53 | Noen ganger (5–29 %) | I 1 tilstand |
| XPO1exportin 1 | Noen ganger (5–29 %) | I 1 tilstand |
| COQ8Acoenzyme Q8A | Sjelden (1–4%) | I 1 tilstand |
| SPTBN1spectrin beta, non-erythrocytic 1 | Sjelden (1–4%) | I 1 tilstand |
| CYP21A2cytochrome P450 family 21 subfamily A member 2 | Ikke registrert | I 1 tilstand |
| ITGA3integrin subunit alpha 3 | Ikke registrert | I 1 tilstand |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Ikke registrert | I 1 tilstand |
| RSPO1R-spondin 1 | Ikke registrert | I 1 tilstand |
| STK11serine/threonine kinase 11 | Ikke registrert | I 1 tilstand |
Hvor ofte dette forekommer hos personer med en av genets tilstander, oppgitt som den hyppigste forekomsten blant dem, slik Human Phenotype Ontology registrerer den. Disse sidene beskriver egenskaper og forskningen bak dem. De er ikke en diagnose, og om symptomer bør du spørre lege eller genetisk rådgiver.
Bredere egenskaper
Slik er informasjonen samlet
- Human Phenotype Ontology, versjon 2026-09-01: egenskapen, navnene på den, definisjonen og genene som er knyttet til den. Les mer på hpo.jax.org.
- Datautgave 2026.10.19-9814e911.
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