Tratto
Abnormal shape of end part of bone
Nome clinico: Abnormal epiphysis morphology
An anomaly of epiphysis, which is the expanded articular end of a long bone that developes from a secondary ossification center, and which during the period of growth is either entirely cartilaginous or is separated from the shaft by a cartilaginous disk.
Riepilogo
- Detto anche
- Abnormality of epiphysis morphology, Abnormality of the epiphyses, Anomaly of the epiphyses, Epiphyseal abnormality
- Sistema corporeo
- Abnormality of the musculoskeletal system
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page$trait$nameLeggi i geni collegati a Abnormal shape of end part of bone e il resto del tuo genoma con un unico test.
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Ottieni il mio Genome Test58 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.
- Zellweger Spectrum & Peroxisome Biogenesis DisordersReads 14 of these genesPEX7PEX1PEX10PEX11BPEX12PEX13About this report →
- Other Inherited LeukodystrophiesReads 16 of these genesTREM2TYROBPPEX7PEX1PEX10PEX11BAbout this report →
- Congenital HypothyroidismReads 8 of these genesDUOX2DUOXA2IYDSLC5A5TGTPOAbout this report →
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 5 of these genesCOL9A1COL9A2COL9A3SLC26A2COL2A1About this report →
Show 54 more reports
- Achondrogenesis panelReads 3 of these genesGDF5SLC26A2COL2A1About this report →
- Thyroid CancerReads 8 of these genesDUOX2DUOXA2IYDSLC5A5TGTPOAbout this report →
- OsteopetrosisReads 5 of these genesCLCN7OSTM1SNX10TCIRG1TNFSF11About this report →
- Rare Hereditary Peripheral NeuropathiesReads 18 of these genesKIF1ARETREG1SCN9AWNK1PEX7PEX1About this report →
- Immuno-Osseous DysplasiasReads 2 of these genesRMRPRNU4ATACAbout this report →
- Adult-Onset Leukodystrophies (CSF1R, LMNB1, Nasu-Hakola)Reads 2 of these genesTREM2TYROBPAbout this report →
- ACAN-Related Short StatureReads 1 of these genesACANAbout this report →
- Catel-Manzke SyndromeReads 1 of these genesTGDSAbout this report →
- CLCN7-Related Hypopigmentation, Organomegaly and Delayed Myelination (HOD)Reads 1 of these genesCLCN7About this report →
- Dyssegmental Dysplasia, Silverman-Handmaker TypeReads 1 of these genesHSPG2About this report →
- Meier-Gorlin Syndrome 3 (ORC6)Reads 1 of these genesORC6About this report →
- Meier-Gorlin Syndrome 4Reads 1 of these genesCDT1About this report →
- Meier-Gorlin Syndrome 7 (CDC45)Reads 1 of these genesCDC45About this report →
- Microcephalic Osteodysplastic Primordial Dwarfism Type IIReads 1 of these genesPCNTAbout this report →
- Mucopolysaccharidosis Type I (Hurler and Scheie Syndromes)Reads 1 of these genesIDUAAbout this report →
- OpsismodysplasiaReads 1 of these genesINPPL1About this report →
- Primary Failure of Tooth EruptionReads 1 of these genesPTH1RAbout this report →
- RNU4ATAC Spectrum DisorderReads 1 of these genesRNU4ATACAbout this report →
- Schwartz-Jampel Syndrome Type 1Reads 1 of these genesHSPG2About this report →
- SHOX Deficiency (Leri-Weill and Langer Dysplasia)Reads 1 of these genesSHOXAbout this report →
- Spondylometaphyseal Dysplasia With Cone-Rod DystrophyReads 1 of these genesPCYT1AAbout this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 5 of these genesHESX1LHX3LHX4POU1F1PROP1About this report →
- Inherited Neurodegenerative DisordersReads 17 of these genesKIF1ATREM2TYROBPPEX7PEX1PEX10About this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 4 of these genesKIF1ARETREG1SCN9AWNK1About this report →
- VitreoretinopathyReads 4 of these genesCOL9A1COL9A2COL9A3COL2A1About this report →
- Cleidocranial DysplasiaReads 1 of these genesRUNX2About this report →
- Dent Disease and Lowe SyndromeReads 1 of these genesOCRLAbout this report →
- FLNB-Related Skeletal Dysplasia (Larsen Spectrum)Reads 1 of these genesFLNBAbout this report →
- Juvenile Polyposis SyndromeReads 1 of these genesSMAD4About this report →
- Otospondylomegaepiphyseal Dysplasia (OSMED)Reads 1 of these genesCOL2A1About this report →
- Hypogonadotropic HypogonadismReads 5 of these genesHESX1LHX3LHX4POU1F1PROP1About this report →
- HyperthyroidismReads 1 of these genesTSHRAbout this report →
- Cutis LaxaReads 2 of these genesGORABPYCR1About this report →
- Hereditary Hemorrhagic TelangiectasiaReads 1 of these genesSMAD4About this report →
- Multiple Synostoses Syndrome (FGF9)Reads 1 of these genesGDF5About this report →
- Alzheimer diseaseReads 1 of these genesTREM2About this report →
- Ehlers-Danlos SyndromeReads 2 of these genesPRDM5ZNF469About this report →
- Peroxisomal Enzyme Disorders & Refsum DiseaseReads 1 of these genesPHYHAbout this report →
- Congenital Cranial Dysinnervation DisordersReads 1 of these genesMAFBAbout this report →
- Hereditary Rickets (Hypophosphatemic and Vitamin D-Dependent)Reads 1 of these genesPHEXAbout this report →
- Osteogenesis ImperfectaReads 2 of these genesGORABPYCR1About this report →
- Marfan Like SyndromesReads 1 of these genesFBN1About this report →
- Aortic AneurysmReads 1 of these genesFBN1About this report →
- Intellectual DisabilityReads 4 of these genesKIF1APIGLSMAD4SMARCA2About this report →
- Monogenic Hypertension & Mineralocorticoid DisordersReads 1 of these genesWNK1About this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPIGLAbout this report →
- Noonan SyndromeReads 1 of these genesPTPN11About this report →
- Congenital Disorders of GlycosylationReads 2 of these genesPIGLGORABAbout this report →
- Epilepsy (Full Panel)Reads 2 of these genesSCN9AUFSP2About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesPEX6About this report →
- Lysosomal Storage DiseaseReads 1 of these genesIDUAAbout this report →
- Hypertrophic CardiomyopathyReads 1 of these genesPTPN11About this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesKIF1AAbout this report →
- Other Inborn Errors of ImmunityReads 1 of these genesRMRPAbout this report →
Leggi i geni collegati a Abnormal shape of end part of bone e il resto del tuo genoma con un unico test.
A partire da 449 $Spedizione gratuita · Risultati in 6–8 settimane
Ottieni il mio Genome Test90 geni collegati a Abnormal shape of end part of bone
Alterazioni in questi geni causano malattie rare in cui si osserva Abnormal shape of end part of bone. La maggior parte delle persone con questo tratto non presenta nessuna di tali condizioni, e un gene di questo elenco non dice nulla sul genoma di nessuno in particolare.
| Gene | Frequenza di osservazione | Condizioni |
|---|---|---|
| ACANaggrecan | Molto spesso (80–99%) | In 1 condizione |
| BMPR1Bbone morphogenetic protein receptor type 1B | Molto spesso (80–99%) | In 1 condizione |
| CDC45cell division cycle 45 | Molto spesso (80–99%) | In 1 condizione |
| CDC6cell division cycle 6 | Molto spesso (80–99%) | In 1 condizione |
| CDT1chromatin licensing and DNA replication factor 1 | Molto spesso (80–99%) | In 1 condizione |
| CLCN7Cl-/H+ antiporter 7 | Molto spesso (80–99%) | In 2 condizioni |
| COL9A1collagen type IX alpha 1 chain | Molto spesso (80–99%) | In 2 condizioni |
| COL9A2collagen type IX alpha 2 chain | Molto spesso (80–99%) | In 2 condizioni |
| COL9A3collagen type IX alpha 3 chain | Molto spesso (80–99%) | In 2 condizioni |
| GDF5growth differentiation factor 5 | Molto spesso (80–99%) | In 2 condizioni |
| GMNNgeminin DNA replication inhibitor | Molto spesso (80–99%) | In 1 condizione |
| HPGD15-hydroxyprostaglandin dehydrogenase | Molto spesso (80–99%) | In 1 condizione |
| HSPG2heparan sulfate proteoglycan 2 | Molto spesso (80–99%) | In 1 condizione |
| INPPL1inositol polyphosphate phosphatase like 1 | Molto spesso (80–99%) | In 1 condizione |
| KIF1Akinesin family member 1A | Molto spesso (80–99%) | In 1 condizione |
| LMBR1limb development membrane protein 1 | Molto spesso (80–99%) | In 1 condizione |
| LONP1lon peptidase 1, mitochondrial | Molto spesso (80–99%) | In 1 condizione |
| MMP13matrix metallopeptidase 13 | Molto spesso (80–99%) | In 2 condizioni |
| MMP9matrix metallopeptidase 9 | Molto spesso (80–99%) | In 1 condizione |
| ORC1origin recognition complex subunit 1 | Molto spesso (80–99%) | In 1 condizione |
| ORC4origin recognition complex subunit 4 | Molto spesso (80–99%) | In 1 condizione |
| ORC6origin recognition complex subunit 6 | Molto spesso (80–99%) | In 1 condizione |
| OSTM1osteoclastogenesis associated transmembrane protein 1 | Molto spesso (80–99%) | In 1 condizione |
| PCNTpericentrin | Molto spesso (80–99%) | In 1 condizione |
| PCYT1Aphosphate cytidylyltransferase 1A, choline | Molto spesso (80–99%) | In 1 condizione |
| PTH1Rparathyroid hormone 1 receptor | Molto spesso (80–99%) | In 1 condizione |
| PTPN11protein tyrosine phosphatase non-receptor type 11 | Molto spesso (80–99%) | In 1 condizione |
| RETREG1reticulophagy regulator 1 | Molto spesso (80–99%) | In 1 condizione |
| RMRPRNA component of mitochondrial RNA processing endoribonuclease | Molto spesso (80–99%) | In 1 condizione |
| RNU4ATACRNA, U4atac small nuclear | Molto spesso (80–99%) | In 1 condizione |
| SCN9Asodium voltage-gated channel alpha subunit 9 | Molto spesso (80–99%) | In 1 condizione |
| SHOXSHOX homeobox | Molto spesso (80–99%) | In 2 condizioni |
| SLC26A2solute carrier family 26 member 2 | Molto spesso (80–99%) | In 1 condizione |
| SLCO2A1solute carrier organic anion transporter family member 2A1 | Molto spesso (80–99%) | In 1 condizione |
| SNX10sorting nexin 10 | Molto spesso (80–99%) | In 1 condizione |
| TBX4T-box transcription factor 4 | Molto spesso (80–99%) | In 2 condizioni |
| TCIRG1T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 | Molto spesso (80–99%) | In 1 condizione |
| TGDSTDP-glucose 4,6-dehydratase | Molto spesso (80–99%) | In 1 condizione |
| TNFSF11TNF superfamily member 11 | Molto spesso (80–99%) | In 1 condizione |
| TREM2triggering receptor expressed on myeloid cells 2 | Molto spesso (80–99%) | In 1 condizione |
Mostra altri 50 geni
| Gene | Frequenza di osservazione | Condizioni |
|---|---|---|
| TYROBPtransmembrane immune signaling adaptor TYROBP | Molto spesso (80–99%) | In 1 condizione |
| UFSP2UFM1 specific peptidase 2 | Molto spesso (80–99%) | In 1 condizione |
| WNK1WNK lysine deficient protein kinase 1 | Molto spesso (80–99%) | In 1 condizione |
| COL2A1collagen type II alpha 1 chain | Spesso (30–79%) | In 1 condizione |
| DDRGK1DDRGK domain containing 1 | Spesso (30–79%) | In 1 condizione |
| DUOX2dual oxidase 2 | Spesso (30–79%) | In 1 condizione |
| DUOXA2dual oxidase maturation factor 2 | Spesso (30–79%) | In 1 condizione |
| ERI1exoribonuclease 1 | Spesso (30–79%) | In 1 condizione |
| HESX1HESX homeobox 1 | Spesso (30–79%) | In 1 condizione |
| IDUAalpha-L-iduronidase | Spesso (30–79%) | In 1 condizione |
| IYDiodotyrosine deiodinase | Spesso (30–79%) | In 1 condizione |
| LHX3LIM homeobox 3 | Spesso (30–79%) | In 1 condizione |
| LHX4LIM homeobox 4 | Spesso (30–79%) | In 1 condizione |
| LOXL3lysyl oxidase like 3 | Spesso (30–79%) | In 1 condizione |
| PEX7peroxisomal biogenesis factor 7 | Spesso (30–79%) | In 1 condizione |
| PHEXphosphate regulating endopeptidase X-linked | Spesso (30–79%) | In 1 condizione |
| PHYHphytanoyl-CoA 2-hydroxylase | Spesso (30–79%) | In 1 condizione |
| PIGLphosphatidylinositol glycan anchor biosynthesis class L | Spesso (30–79%) | In 1 condizione |
| POU1F1POU class 1 homeobox 1 | Spesso (30–79%) | In 1 condizione |
| PROP1PROP paired-like homeobox 1 | Spesso (30–79%) | In 1 condizione |
| SLC5A5solute carrier family 5 member 5 | Spesso (30–79%) | In 1 condizione |
| SMAD4SMAD family member 4 | Spesso (30–79%) | In 1 condizione |
| TGthyroglobulin | Spesso (30–79%) | In 1 condizione |
| TPOthyroid peroxidase | Spesso (30–79%) | In 1 condizione |
| TSHBthyroid stimulating hormone subunit beta | Spesso (30–79%) | In 1 condizione |
| FBN1fibrillin 1 | A volte (5–29%) | In 1 condizione |
| FLNBfilamin B | A volte (5–29%) | In 1 condizione |
| GORABgolgin, RAB6 interacting | A volte (5–29%) | In 1 condizione |
| LTBP3latent transforming growth factor beta binding protein 3 | A volte (5–29%) | In 1 condizione |
| MAFBMAF bZIP transcription factor B | A volte (5–29%) | In 1 condizione |
| OCRLOCRL inositol polyphosphate-5-phosphatase | A volte (5–29%) | In 1 condizione |
| PEX1peroxisomal biogenesis factor 1 | A volte (5–29%) | In 1 condizione |
| PEX10peroxisomal biogenesis factor 10 | A volte (5–29%) | In 1 condizione |
| PEX11Bperoxisomal biogenesis factor 11 beta | A volte (5–29%) | In 1 condizione |
| PEX12peroxisomal biogenesis factor 12 | A volte (5–29%) | In 1 condizione |
| PEX13peroxisomal biogenesis factor 13 | A volte (5–29%) | In 1 condizione |
| PEX14peroxisomal biogenesis factor 14 | A volte (5–29%) | In 1 condizione |
| PEX16peroxisomal biogenesis factor 16 | A volte (5–29%) | In 1 condizione |
| PEX19peroxisomal biogenesis factor 19 | A volte (5–29%) | In 1 condizione |
| PEX2peroxisomal biogenesis factor 2 | A volte (5–29%) | In 1 condizione |
| PEX26peroxisomal biogenesis factor 26 | A volte (5–29%) | In 1 condizione |
| PEX3peroxisomal biogenesis factor 3 | A volte (5–29%) | In 1 condizione |
| PEX5peroxisomal biogenesis factor 5 | A volte (5–29%) | In 1 condizione |
| PEX6peroxisomal biogenesis factor 6 | A volte (5–29%) | In 1 condizione |
| PRDM5PR/SET domain 5 | A volte (5–29%) | In 1 condizione |
| PYCR1pyrroline-5-carboxylate reductase 1 | A volte (5–29%) | In 1 condizione |
| RUNX2RUNX family transcription factor 2 | A volte (5–29%) | In 1 condizione |
| SMARCA2SWI/SNF related BAF chromatin remodeling complex subunit ATPase 2 | A volte (5–29%) | In 1 condizione |
| TSHRthyroid stimulating hormone receptor | A volte (5–29%) | In 1 condizione |
| ZNF469zinc finger protein 469 | A volte (5–29%) | In 1 condizione |
Con quale frequenza questo tratto si presenta tra le persone con una delle condizioni legate al gene, nella misura più alta riscontrata tra queste, secondo quanto registrato dall'Human Phenotype Ontology. Queste pagine descrivono tratti e la ricerca che li riguarda; non costituiscono una diagnosi, e per i sintomi il medico o il consulente genetico è la persona a cui rivolgersi.
Tratti più specifici
- Cone-shaped end part of bone66 geni
- Speckled calcifications in end part of bone34 geni
- Abnormal development of end part of bone31 geni
- Delayed maturation of end part of long bone26 geni
- Small end part of bone20 geni
- Flat end part of bone17 geni
- Irregular end part of long bone17 geni
- Large end part of bone7 geni
- Increased bone density in end part of bone3 geni
- Pseudoepiphyses3 geni
- Abnormal shape of the end part of the vertebra bone2 geni
- Epiphyseal deformities of tubular bones2 geni
- Fragmented end part of bone2 geni
- Absent end part of bone1 gene
- Multinucleated giant chondrocytes in epiphyseal cartilage1 gene
- Splayed end part of bone1 gene
- Abnormal shape of end part of limb bones
- Triangular end part of bone
Tratti più generali
Fonte dei dati
- Human Phenotype Ontology, versione 2026-09-01: il tratto, i suoi nomi, la sua definizione e i geni a esso collegati. Per saperne di più visiti hpo.jax.org.
- Versione dei dati 2026.10.19-9814e911.
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