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Merkmal
Enlarged male breast
Klinische Bezeichnung: Gynecomastia
Abnormal development of large mammary glands in males resulting in breast enlargement.
Zusammenfassung
- Auch genannt
- Gynaecomastia
- Körpersystem
- Abnormality of the breast
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Diese Seite als Daten
Hängen Sie .json an die Adresse der Seite an oder fordern Sie application/json an, um sie als JSON zu lesen.
library(jsonlite)
url <- "https://dantelabs.com/traits/gynecomastia.json"
page <- fromJSON(url)
page$trait$nameEnlarged male breastHP:0000771
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AnmeldenFragenIhr Genom sequenzieren↗
Lesen Sie die Gene aus, die mit Enlarged male breast zusammenhängen, und den Rest Ihres Genoms, mit einem einzigen Test.
Ab 449 $Kostenloser Versand · Ergebnisse in 6–8 Wochen
Meinen Genome Test bestellen73 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 →
Lesen Sie die Gene aus, die mit Enlarged male breast zusammenhängen, und den Rest Ihres Genoms, mit einem einzigen Test.
Ab 449 $Kostenloser Versand · Ergebnisse in 6–8 Wochen
Meinen Genome Test bestellen99 Gene mit Enlarged male breast verknüpft
Veränderungen in diesen Genen verursachen seltene Erkrankungen, bei denen Enlarged male breast auftritt. Die meisten Menschen mit diesem Merkmal haben keine dieser Erkrankungen, und ein Gen auf dieser Liste sagt nichts über das eigene Genom einer Person aus.
| Gen | Wie häufig es auftritt | Erkrankungen |
|---|---|---|
| PLAAT3phospholipase A and acyltransferase 3 | Immer | In 1 Erkrankung |
| RFC4replication factor C subunit 4 | Immer | In 1 Erkrankung |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Immer | In 1 Erkrankung |
| AKT2AKT serine/threonine kinase 2 | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| ARandrogen receptor | Sehr häufig (80–99 %) | In 5 Erkrankungen |
| CYP11A1cytochrome P450 family 11 subfamily A member 1 | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| CYP19A1cytochrome P450 family 19 subfamily A member 1 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| DHX37DEAH-box helicase 37 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| GATA4GATA binding protein 4 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| HDAC8histone deacetylase 8 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| LAS1LLAS1 like ribosome biogenesis factor | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| LEPleptin | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| LEPRleptin receptor | Sehr häufig (80–99 %) | In 1 Erkrankung |
| MAP3K1mitogen-activated protein kinase kinase kinase 1 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| NR0B1nuclear receptor subfamily 0 group B member 1 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| NR5A1nuclear receptor subfamily 5 group A member 1 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| PHF6PHD finger protein 6 | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| PNPLA6patatin like domain 6, lysophospholipase | Sehr häufig (80–99 %) | In 1 Erkrankung |
| RBM28RNA binding motif protein 28 | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| RNF216ring finger protein 216 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| SOX9SRY-box transcription factor 9 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| SRYsex determining region Y | Sehr häufig (80–99 %) | In 3 Erkrankungen |
| VAMP7vesicle associated membrane protein 7 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| WT1WT1 transcription factor | Sehr häufig (80–99 %) | In 1 Erkrankung |
| WWOXWW domain containing oxidoreductase | Sehr häufig (80–99 %) | In 1 Erkrankung |
| ZFPM2zinc finger protein, FOG family member 2 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| AIPAHR interacting HSP90 co-chaperone | Häufig (30–79 %) | In 1 Erkrankung |
| CDH23cadherin related 23 | Häufig (30–79 %) | In 2 Erkrankungen |
| CHD7chromodomain helicase DNA binding protein 7 | Häufig (30–79 %) | In 2 Erkrankungen |
| CPEcarboxypeptidase E | Häufig (30–79 %) | In 1 Erkrankung |
| CUL4Bcullin 4B | Häufig (30–79 %) | In 1 Erkrankung |
| CYP17A1cytochrome P450 family 17 subfamily A member 1 | Häufig (30–79 %) | In 3 Erkrankungen |
| DESdesmin | Häufig (30–79 %) | In 1 Erkrankung |
| DUSP6dual specificity phosphatase 6 | Häufig (30–79 %) | In 2 Erkrankungen |
| EMX2empty spiracles homeobox 2 | Häufig (30–79 %) | In 2 Erkrankungen |
| FGF17fibroblast growth factor 17 | Häufig (30–79 %) | In 2 Erkrankungen |
| FGF8fibroblast growth factor 8 | Häufig (30–79 %) | In 2 Erkrankungen |
| FGFR1fibroblast growth factor receptor 1 | Häufig (30–79 %) | In 3 Erkrankungen |
| FMR1fragile X messenger ribonucleoprotein 1 | Häufig (30–79 %) | In 1 Erkrankung |
| GNRH1gonadotropin releasing hormone 1 | Häufig (30–79 %) | In 1 Erkrankung |
59 weitere Gene anzeigen
| Gen | Wie häufig es auftritt | Erkrankungen |
|---|---|---|
| GNRHRgonadotropin releasing hormone receptor | Häufig (30–79 %) | In 1 Erkrankung |
| HS6ST1heparan sulfate 6-O-sulfotransferase 1 | Häufig (30–79 %) | In 2 Erkrankungen |
| HSD3B2hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2 | Häufig (30–79 %) | In 1 Erkrankung |
| KISS1KiSS-1 metastasis suppressor | Häufig (30–79 %) | In 1 Erkrankung |
| KISS1RKISS1 receptor | Häufig (30–79 %) | In 2 Erkrankungen |
| LHBluteinizing hormone subunit beta | Häufig (30–79 %) | In 1 Erkrankung |
| MEN1menin 1 | Häufig (30–79 %) | In 1 Erkrankung |
| NHLH2nescient helix-loop-helix 2 | Häufig (30–79 %) | In 1 Erkrankung |
| NSMFNMDA receptor synaptonuclear signaling and neuronal migration factor | Häufig (30–79 %) | In 2 Erkrankungen |
| PROK2prokineticin 2 | Häufig (30–79 %) | In 2 Erkrankungen |
| PROKR2prokineticin receptor 2 | Häufig (30–79 %) | In 2 Erkrankungen |
| SLC29A3solute carrier family 29 member 3 | Häufig (30–79 %) | In 2 Erkrankungen |
| SMCHD1structural maintenance of chromosomes flexible hinge domain containing 1 | Häufig (30–79 %) | In 1 Erkrankung |
| SPRY4sprouty RTK signaling antagonist 4 | Häufig (30–79 %) | In 2 Erkrankungen |
| TAC3tachykinin precursor 3 | Häufig (30–79 %) | In 1 Erkrankung |
| TACR3tachykinin receptor 3 | Häufig (30–79 %) | In 2 Erkrankungen |
| TCF20transcription factor 20 | Häufig (30–79 %) | In 1 Erkrankung |
| TTI1TELO2 interacting protein 1 | Häufig (30–79 %) | In 1 Erkrankung |
| WDR11WD repeat domain 11 | Häufig (30–79 %) | In 2 Erkrankungen |
| ZBTB20zinc finger and BTB domain containing 20 | Häufig (30–79 %) | In 2 Erkrankungen |
| AFF4ALF transcription elongation factor 4 | Manchmal (5–29 %) | In 1 Erkrankung |
| ALMS1ALMS1 centrosome and basal body associated protein | Manchmal (5–29 %) | In 2 Erkrankungen |
| ANOS1anosmin 1 | Manchmal (5–29 %) | In 2 Erkrankungen |
| BCL11ABCL11 transcription factor A | Manchmal (5–29 %) | In 1 Erkrankung |
| BMP6bone morphogenetic protein 6 | Manchmal (5–29 %) | In 1 Erkrankung |
| CCDC141coiled-coil domain containing 141 | Manchmal (5–29 %) | In 1 Erkrankung |
| CYB5Acytochrome b5 type A | Manchmal (5–29 %) | In 1 Erkrankung |
| CYP11B1cytochrome P450 family 11 subfamily B member 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| DCCDCC netrin 1 receptor | Manchmal (5–29 %) | In 1 Erkrankung |
| ERMARDER membrane associated RNA degradation | Manchmal (5–29 %) | In 1 Erkrankung |
| FEZF1FEZ family zinc finger 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| FLRT3fibronectin leucine rich transmembrane protein 3 | Manchmal (5–29 %) | In 1 Erkrankung |
| HESX1HESX homeobox 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| HFEhomeostatic iron regulator | Manchmal (5–29 %) | In 1 Erkrankung |
| HPGD15-hydroxyprostaglandin dehydrogenase | Manchmal (5–29 %) | In 1 Erkrankung |
| HSD17B3hydroxysteroid 17-beta dehydrogenase 3 | Manchmal (5–29 %) | In 2 Erkrankungen |
| IL17RDinterleukin 17 receptor D | Manchmal (5–29 %) | In 1 Erkrankung |
| MECP2methyl-CpG binding protein 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| NDNFneuron derived neurotrophic factor | Manchmal (5–29 %) | In 1 Erkrankung |
| PDE11Aphosphodiesterase 11A | Manchmal (5–29 %) | In 1 Erkrankung |
| POLR3ARNA polymerase III subunit A | Manchmal (5–29 %) | In 2 Erkrankungen |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Manchmal (5–29 %) | In 1 Erkrankung |
| PSMB8proteasome 20S subunit beta 8 | Manchmal (5–29 %) | In 1 Erkrankung |
| PTENphosphatase and tensin homolog | Manchmal (5–29 %) | In 2 Erkrankungen |
| RELREL proto-oncogene, NF-kB subunit | Manchmal (5–29 %) | In 1 Erkrankung |
| SEMA3Asemaphorin 3A | Manchmal (5–29 %) | In 1 Erkrankung |
| SH3PXD2BSH3 and PX domains 2B | Manchmal (5–29 %) | In 1 Erkrankung |
| SLCO2A1solute carrier organic anion transporter family member 2A1 | Manchmal (5–29 %) | In 1 Erkrankung |
| SMC5structural maintenance of chromosomes 5 | Manchmal (5–29 %) | In 1 Erkrankung |
| SOX10SRY-box transcription factor 10 | Manchmal (5–29 %) | In 1 Erkrankung |
| TMEM53transmembrane protein 53 | Manchmal (5–29 %) | In 1 Erkrankung |
| XPO1exportin 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| COQ8Acoenzyme Q8A | Selten (1–4 %) | In 1 Erkrankung |
| SPTBN1spectrin beta, non-erythrocytic 1 | Selten (1–4 %) | In 1 Erkrankung |
| CYP21A2cytochrome P450 family 21 subfamily A member 2 | Nicht erfasst | In 1 Erkrankung |
| ITGA3integrin subunit alpha 3 | Nicht erfasst | In 1 Erkrankung |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Nicht erfasst | In 1 Erkrankung |
| RSPO1R-spondin 1 | Nicht erfasst | In 1 Erkrankung |
| STK11serine/threonine kinase 11 | Nicht erfasst | In 1 Erkrankung |
Wie häufig dieses Merkmal bei Menschen mit einer der Erkrankungen auftritt, die mit dem Gen in Verbindung stehen, und zwar der höchste Wert unter ihnen, so wie ihn die Human Phenotype Ontology erfasst. Diese Seiten beschreiben Merkmale und die dazugehörige Forschung; sie stellen keine Diagnose dar. Fragen zu Symptomen richten Sie bitte an Ihre Ärztin, Ihren Arzt oder eine genetische Beratung.
Übergeordnete Merkmale
Woher diese Angaben stammen
- Die Human Phenotype Ontology, Version 2026-09-01: das Merkmal, seine Bezeichnungen, seine Definition und die damit verknüpften Gene. Weitere Informationen finden Sie unter hpo.jax.org.
- Datenstand 2026.10.19-9814e911.
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