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Cecha
Short chin
Decreased vertical distance from the vermilion border of the lower lip to the inferior-most point of the chin.
Podsumowanie
- Znana także jako
- Decreased height of chin, Short lower third of face, Small chin, Vertical deficiency of chin, Vertical hypoplasia of chin
- Układ organizmu
- Abnormality of head or neck
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Ta strona jako dane
Aby odczytać ją jako JSON, dodaj .json na końcu adresu strony lub zażądaj application/json.
library(jsonlite)
url <- "https://dantelabs.com/traits/short-chin.json"
page <- fromJSON(url)
page$trait$nameShort chinHP:0000331
AtlasKomu pomagamyNasza naukaProduktyWyniki
Zaloguj sięZapytajZsekwencjonuj swój genom↗
Odczytaj geny powiązane z Short chin oraz resztę swojego genomu za pomocą jednego badania.
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Zamawiam Genome Test59 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.
- Intellectual DisabilityReads 21 of these genesHIVEP2NSD2TAF4AP1S2ASXL3CDK10About this report →
- EBF3-Related Neurodevelopmental Disorder (HADDS)Reads 1 of these genesEBF3About this report →
- ITCH DeficiencyReads 1 of these genesITCHAbout this report →
- Jaberi-Elahi SyndromeReads 1 of these genesGTPBP2About this report →
Show 55 more reports
- NFIA-Related Brain MalformationsReads 1 of these genesNFIAAbout this report →
- PIK3R1-Related DisordersReads 1 of these genesPIK3R1About this report →
- PPP1R21-Related Neurodevelopmental DisorderReads 1 of these genesPPP1R21About this report →
- Restrictive Dermopathy (ZMPSTE24)Reads 1 of these genesZMPSTE24About this report →
- RNU4ATAC Spectrum DisorderReads 1 of these genesRNU4ATACAbout this report →
- Spondylo-Meta-Epiphyseal Dysplasia, Short Limb-Abnormal Calcification TypeReads 1 of these genesDDR2About this report →
- Activated PI3K-Delta Syndrome (APDS)Reads 1 of these genesPIK3R1About this report →
- Cowden Syndrome (PTEN hamartoma tumour syndrome)Reads 1 of these genesPTENAbout this report →
- Hereditary Mixed Polyposis SyndromeReads 1 of these genesBMPR1AAbout this report →
- Juvenile Polyposis SyndromeReads 1 of these genesBMPR1AAbout this report →
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 2 of these genesCOL9A2SLC26A2About this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 2 of these genesH19IGF2About this report →
- DNA Repair DiseaseReads 4 of these genesERCC1ERCC4ERCC6ERCC8About this report →
- Coffin-Siris SyndromeReads 2 of these genesSOX11ARID1BAbout this report →
- LipodystrophyReads 2 of these genesLMNAZMPSTE24About this report →
- Congenital Diaphragmatic Hernia (Monogenic)Reads 1 of these genesALDH1A2About this report →
- Immuno-Osseous DysplasiasReads 1 of these genesRNU4ATACAbout this report →
- Rothmund-Thomson SyndromeReads 1 of these genesRECQL4About this report →
- Achondrogenesis panelReads 1 of these genesSLC26A2About this report →
- Complex Neurodevelopmental Disorder (TRRAP, MYH10, RERE, SOX11)Reads 1 of these genesSOX11About this report →
- Mosaic Variegated Aneuploidy SyndromeReads 1 of these genesSLF2About this report →
- MTOR Pathway Megalencephaly and Overgrowth DisordersReads 1 of these genesMTORAbout this report →
- Periventricular Nodular HeterotopiaReads 1 of these genesFLNAAbout this report →
- Syndromic Complex Neurodevelopmental DisorderReads 2 of these genesAP1S2RNU4-2About this report →
- Cornelia de Lange SyndromeReads 1 of these genesSMC3About this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 1 of these genesFLNAAbout this report →
- Microphthalmia, Anophthalmia & ColobomaReads 2 of these genesCOX7BERCC1About this report →
- Hypodontia and AnodontiaReads 1 of these genesEDAAbout this report →
- Epilepsy (Full Panel)Reads 5 of these genesRNF13ALG13PIGSFLNAPARS2About this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 5 of these genesFBXL4LMNADSTFIG4NDUFS4About this report →
- Agammaglobulinaemia (XLA and Autosomal Forms)Reads 1 of these genesPIK3R1About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesFLNAAbout this report →
- Primary Mitochondrial DiseaseReads 3 of these genesCOA6FBXL4NDUFS4About this report →
- Hypertrophic CardiomyopathyReads 2 of these genesH19IGF2About this report →
- Leigh SyndromeReads 2 of these genesFBXL4NDUFS4About this report →
- Ectodermal DysplasiasReads 1 of these genesEDAAbout this report →
- Fanconi AnemiaReads 1 of these genesERCC4About this report →
- Epidermolysis BullosaReads 1 of these genesDSTAbout this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesLMNAFIG4About this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPIGSAbout this report →
- Neonatal Diabetes MellitusReads 1 of these genesPTF1AAbout this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 1 of these genesDSTAbout this report →
- Dyskeratosis CongenitaReads 1 of these genesZBTB24About this report →
- Syndromic CraniosynostosisReads 1 of these genesRECQL4About this report →
- Congenital Disorders of GlycosylationReads 2 of these genesALG13MAN1B1About this report →
- VitreoretinopathyReads 1 of these genesCOL9A2About this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 1 of these genesFIG4About this report →
- Diabetes MellitusReads 1 of these genesPTF1AAbout this report →
- Severe Combined ImmunodeficiencyReads 1 of these genesPRKDCAbout this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesLMNAAbout this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesVAC14About this report →
- Dilated CardiomyopathyReads 1 of these genesLMNAAbout this report →
- Other Inborn Errors of ImmunityReads 2 of these genesPIK3R1PRKDCAbout this report →
- Inherited Neurodegenerative DisordersReads 2 of these genesFIG4VAC14About this report →
Odczytaj geny powiązane z Short chin oraz resztę swojego genomu za pomocą jednego badania.
Od 449 $Bezpłatna wysyłka · Wyniki w ciągu 6–8 tygodni
Zamawiam Genome Test77 genów powiązanych z Short chin
Zmiany w tych genach powodują rzadkie choroby, w których występuje Short chin. Większość osób z tą cechą nie ma żadnej z tych chorób, a gen z tej listy nic nie mówi o czyimkolwiek własnym genomie.
| Gen | Jak często występuje | Choroby |
|---|---|---|
| COA6cytochrome c oxidase assembly factor 6 | Zawsze | W 1 chorobie |
| COL9A2collagen type IX alpha 2 chain | Zawsze | W 1 chorobie |
| FBXL4F-box and leucine rich repeat protein 4 | Zawsze | W 1 chorobie |
| GTPBP2GTP binding protein 2 | Zawsze | W 1 chorobie |
| HIVEP2HIVEP zinc finger 2 | Zawsze | W 1 chorobie |
| ITCHitchy E3 ubiquitin protein ligase | Zawsze | W 2 chorobach |
| LMNAlamin A/C | Zawsze | W 2 chorobach |
| MAN2B2mannosidase alpha class 2B member 2 | Zawsze | W 1 chorobie |
| NSD2nuclear receptor binding SET domain protein 2 | Zawsze | W 1 chorobie |
| PAPPA2pappalysin 2 | Zawsze | W 1 chorobie |
| PIK3R1phosphoinositide-3-kinase regulatory subunit 1 | Zawsze | W 1 chorobie |
| RPL17ribosomal protein L17 | Zawsze | W 1 chorobie |
| SCUBE3signal peptide, CUB domain and EGF like domain containing 3 | Zawsze | W 1 chorobie |
| TAF4TATA-box binding protein associated factor 4 | Zawsze | W 1 chorobie |
| AP1S2adaptor related protein complex 1 subunit sigma 2 | Bardzo często (80–99%) | W 1 chorobie |
| H19H19 imprinted maternally expressed transcript | Bardzo często (80–99%) | W 1 chorobie |
| IGF2insulin like growth factor 2 | Bardzo często (80–99%) | W 1 chorobie |
| PTF1Apancreas associated transcription factor 1a | Bardzo często (80–99%) | W 2 chorobach |
| ABL1ABL proto-oncogene 1, non-receptor tyrosine kinase | Często (30–79%) | W 1 chorobie |
| ALDH1A2aldehyde dehydrogenase 1 family member A2 | Często (30–79%) | W 1 chorobie |
| ASXL3ASXL transcriptional regulator 3 | Często (30–79%) | W 1 chorobie |
| CDK10cyclin dependent kinase 10 | Często (30–79%) | W 1 chorobie |
| COX7Bcytochrome c oxidase subunit 7B | Często (30–79%) | W 1 chorobie |
| CYP26C1cytochrome P450 family 26 subfamily C member 1 | Często (30–79%) | W 1 chorobie |
| DSTdystonin | Często (30–79%) | W 2 chorobach |
| EBF3EBF transcription factor 3 | Często (30–79%) | W 1 chorobie |
| EXTL3exostosin like glycosyltransferase 3 | Często (30–79%) | W 1 chorobie |
| FIG4FIG4 phosphoinositide 5-phosphatase | Często (30–79%) | W 1 chorobie |
| MAP3K7mitogen-activated protein kinase kinase kinase 7 | Często (30–79%) | W 1 chorobie |
| MEF2Cmyocyte enhancer factor 2C | Często (30–79%) | W 1 chorobie |
| MYOD1myogenic differentiation 1 | Często (30–79%) | W 1 chorobie |
| NDUFS4NADH:ubiquinone oxidoreductase subunit S4 | Często (30–79%) | W 1 chorobie |
| PGBD5piggyBac transposable element derived 5 | Często (30–79%) | W 1 chorobie |
| RNF13ring finger protein 13 | Często (30–79%) | W 2 chorobach |
| SLC26A2solute carrier family 26 member 2 | Często (30–79%) | W 1 chorobie |
| SMC3structural maintenance of chromosomes 3 | Często (30–79%) | W 1 chorobie |
| SOX11SRY-box transcription factor 11 | Często (30–79%) | W 1 chorobie |
| VAC14VAC14 component of PIKFYVE complex | Często (30–79%) | W 1 chorobie |
| ADNPactivity dependent neuroprotector homeobox | Czasami (5–29%) | W 1 chorobie |
| AHDC1AT-hook DNA binding motif containing 1 | Czasami (5–29%) | W 1 chorobie |
Pokaż jeszcze 37 genów
| Gen | Jak często występuje | Choroby |
|---|---|---|
| ALG13ALG13 UDP-N-acetylglucosaminyltransferase subunit | Czasami (5–29%) | W 1 chorobie |
| BMPR1Abone morphogenetic protein receptor type 1A | Czasami (5–29%) | W 1 chorobie |
| CAMK2Bcalcium/calmodulin dependent protein kinase II beta | Czasami (5–29%) | W 1 chorobie |
| DDR2discoidin domain receptor tyrosine kinase 2 | Czasami (5–29%) | W 1 chorobie |
| ERCC1ERCC excision repair 1, endonuclease non-catalytic subunit | Czasami (5–29%) | W 1 chorobie |
| ERCC4ERCC excision repair 4, endonuclease catalytic subunit | Czasami (5–29%) | W 1 chorobie |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Czasami (5–29%) | W 3 chorobach |
| ERCC8ERCC excision repair 8, CSA ubiquitin ligase complex subunit | Czasami (5–29%) | W 3 chorobach |
| FBXO31F-box protein 31 | Czasami (5–29%) | W 1 chorobie |
| GRB10growth factor receptor bound protein 10 | Czasami (5–29%) | W 1 chorobie |
| MAN1B1mannosidase alpha class 1B member 1 | Czasami (5–29%) | W 1 chorobie |
| MED12mediator complex subunit 12 | Czasami (5–29%) | W 1 chorobie |
| NRCAMneuronal cell adhesion molecule | Czasami (5–29%) | W 1 chorobie |
| PIGSphosphatidylinositol glycan anchor biosynthesis class S | Czasami (5–29%) | W 1 chorobie |
| PPP1R21protein phosphatase 1 regulatory subunit 21 | Czasami (5–29%) | W 1 chorobie |
| PRKDCprotein kinase, DNA-activated, catalytic subunit | Czasami (5–29%) | W 1 chorobie |
| PTENphosphatase and tensin homolog | Czasami (5–29%) | W 1 chorobie |
| RNU4ATACRNA, U4atac small nuclear | Czasami (5–29%) | W 1 chorobie |
| SETSET nuclear proto-oncogene | Czasami (5–29%) | W 1 chorobie |
| SLF2SMC5/6 complex localization factor 2 | Czasami (5–29%) | W 1 chorobie |
| TRIOtrio Rho guanine nucleotide exchange factor | Czasami (5–29%) | W 2 chorobach |
| ZMPSTE24zinc metallopeptidase STE24 | Czasami (5–29%) | W 1 chorobie |
| ZNF292zinc finger protein 292 | Czasami (5–29%) | W 1 chorobie |
| CTCFCCCTC-binding factor | Rzadko (1–4%) | W 1 chorobie |
| MTORmechanistic target of rapamycin kinase | Rzadko (1–4%) | W 2 chorobach |
| RNU4-2RNA, U4 small nuclear 2 | Rzadko (1–4%) | W 1 chorobie |
| ARID1BAT-rich interaction domain 1B | Nie odnotowano | W 1 chorobie |
| EDAectodysplasin A | Nie odnotowano | W 1 chorobie |
| FLNAfilamin A | Nie odnotowano | W 1 chorobie |
| MBD5methyl-CpG binding domain protein 5 | Nie odnotowano | W 1 chorobie |
| NFIAnuclear factor I A | Nie odnotowano | W 1 chorobie |
| NSUN2NOP2/Sun RNA methyltransferase 2 | Nie odnotowano | W 1 chorobie |
| PARS2prolyl-tRNA synthetase 2, mitochondrial | Nie odnotowano | W 1 chorobie |
| RECQL4RecQ like helicase 4 | Nie odnotowano | W 1 chorobie |
| SHANK3SH3 and multiple ankyrin repeat domains 3 | Nie odnotowano | W 1 chorobie |
| XRCC4X-ray repair cross complementing 4 | Nie odnotowano | W 1 chorobie |
| ZBTB24zinc finger and BTB domain containing 24 | Nie odnotowano | W 1 chorobie |
Jak często występuje wśród osób z jedną z chorób związanych z tym genem, najczęściej spośród wszystkich, według danych Human Phenotype Ontology. Te strony opisują cechy i badania, na których się opierają; nie są diagnozą, a w sprawie objawów należy zwrócić się do lekarza lub doradcy genetycznego.
Cechy nadrzędne
Skąd pochodzą te dane
- Human Phenotype Ontology, wydanie 2026-09-01: cecha, jej nazwy, definicja oraz geny z nią powiązane. Więcej informacji znajdą Państwo na stronie hpo.jax.org.
- Wydanie danych 2026.10.19-9814e911.
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Zaloguj sięZapytajZsekwencjonuj swój genom↗
From traits to your genome
Read the genes behind these traits in your own DNA.
The Genome Test sequences nearly all of your DNA, not a preset panel, so every gene on these pages is in your data. Premium adds 810+ physician-ready reports.
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