AtlasWho We HelpOur ScienceProductsOutcomes
Log InAskSequence your genome↗
Trait
Limb undergrowth
Limb shortening because of underdevelopment of one or more bones of the extremities.
Summary
- Also called
- limb shortening, Short limb, Short limbs, Hypoplasia involving bones of the extremities
AtlasWho We HelpOur ScienceProductsOutcomes
Log InAskSequence your genome↗
This page as data
Add .json to the page's address, or ask for application/json, to read it as JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/limb-undergrowth.json"
page <- fromJSON(url)
page$trait$nameLimb undergrowthHP:0009826
AtlasWho We HelpOur ScienceProductsOutcomes
Log InAskSequence your genome↗
Read the genes linked to Limb undergrowth, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome Test63 genes linked to Limb undergrowth
Changes in these genes cause rare conditions in which Limb undergrowth is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| ADAMTS2ADAM metallopeptidase with thrombospondin type 1 motif 2 | Always | In 2 conditions |
| B9D1B9 domain containing 1 | Always | In 1 condition |
| BMPR1Bbone morphogenetic protein receptor type 1B | Always | In 1 condition |
| CILK1ciliogenesis associated kinase 1 | Always | In 1 condition |
| COL1A1collagen type I alpha 1 chain | Always | In 1 condition |
| COL1A2collagen type I alpha 2 chain | Always | In 1 condition |
| COL2A1collagen type II alpha 1 chain | Always | In 1 condition |
| DDRGK1DDRGK domain containing 1 | Always | In 2 conditions |
| ERI1exoribonuclease 1 | Always | In 1 condition |
| FLNBfilamin B | Always | In 2 conditions |
| FUT8fucosyltransferase 8 | Always | In 1 condition |
| GLB1galactosidase beta 1 | Always | In 1 condition |
| IFT52intraflagellar transport 52 | Always | In 1 condition |
| IHHIndian hedgehog signaling molecule | Always | In 1 condition |
| PLCB3phospholipase C beta 3 | Always | In 1 condition |
| RIPK4receptor interacting serine/threonine kinase 4 | Always | In 1 condition |
| SLC35D1solute carrier family 35 member D1 | Always | In 1 condition |
| COL10A1collagen type X alpha 1 chain | Very often (80–99%) | In 1 condition |
| FGFR3fibroblast growth factor receptor 3 | Very often (80–99%) | In 1 condition |
| MATN3matrilin 3 | Very often (80–99%) | In 1 condition |
| PRKACAprotein kinase cAMP-activated catalytic subunit alpha | Very often (80–99%) | In 1 condition |
| SLC26A2solute carrier family 26 member 2 | Very often (80–99%) | In 2 conditions |
| ADAMTSL2ADAMTS like 2 | Often (30–79%) | In 1 condition |
| COL11A2collagen type XI alpha 2 chain | Often (30–79%) | In 1 condition |
| COL9A1collagen type IX alpha 1 chain | Often (30–79%) | In 1 condition |
| COL9A2collagen type IX alpha 2 chain | Often (30–79%) | In 1 condition |
| COL9A3collagen type IX alpha 3 chain | Often (30–79%) | In 1 condition |
| COMPcartilage oligomeric matrix protein | Often (30–79%) | In 1 condition |
| DLK1delta like non-canonical Notch ligand 1 | Often (30–79%) | In 1 condition |
| EXTL3exostosin like glycosyltransferase 3 | Often (30–79%) | In 2 conditions |
| HSPG2heparan sulfate proteoglycan 2 | Often (30–79%) | In 1 condition |
| LBRlamin B receptor | Often (30–79%) | In 1 condition |
| MEG3maternally expressed 3 | Often (30–79%) | In 1 condition |
| NINninein | Often (30–79%) | In 1 condition |
| PIGYphosphatidylinositol glycan anchor biosynthesis class Y | Often (30–79%) | In 1 condition |
| RTL1retrotransposon Gag like 1 | Often (30–79%) | In 1 condition |
| TBCKTBC1 domain containing kinase | Often (30–79%) | In 2 conditions |
| TONSLtonsoku like, DNA repair protein | Often (30–79%) | In 1 condition |
| ACP5acid phosphatase 5, tartrate resistant | Sometimes (5–29%) | In 1 condition |
| BPNT23'(2'), 5'-bisphosphate nucleotidase 2 | Sometimes (5–29%) | In 1 condition |
Show 23 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| CLTCL1clathrin heavy chain like 1 | Sometimes (5–29%) | In 1 condition |
| DPM1dolichyl-phosphate mannosyltransferase subunit 1, catalytic | Sometimes (5–29%) | In 1 condition |
| EXT1exostosin glycosyltransferase 1 | Sometimes (5–29%) | In 1 condition |
| EXT2exostosin glycosyltransferase 2 | Sometimes (5–29%) | In 1 condition |
| GAD1glutamate decarboxylase 1 | Sometimes (5–29%) | In 1 condition |
| LONP1lon peptidase 1, mitochondrial | Sometimes (5–29%) | In 1 condition |
| NEK1NIMA related kinase 1 | Sometimes (5–29%) | In 1 condition |
| PDHA1pyruvate dehydrogenase E1 subunit alpha 1 | Sometimes (5–29%) | In 1 condition |
| PRKACBprotein kinase cAMP-activated catalytic subunit beta | Sometimes (5–29%) | In 1 condition |
| SLC35C1solute carrier family 35 member C1 | Sometimes (5–29%) | In 1 condition |
| SLC39A8solute carrier family 39 member 8 | Sometimes (5–29%) | In 1 condition |
| FRAS1Fraser extracellular matrix complex subunit 1 | Rarely (1–4%) | In 1 condition |
| FREM2FRAS1 related extracellular matrix 2 | Rarely (1–4%) | In 1 condition |
| GRIP1glutamate receptor interacting protein 1 | Rarely (1–4%) | In 1 condition |
| CD96CD96 molecule | Not recorded | In 1 condition |
| FGFR1fibroblast growth factor receptor 1 | Not recorded | In 1 condition |
| GHRgrowth hormone receptor | Not recorded | In 1 condition |
| GNASGNAS complex locus | Not recorded | In 1 condition |
| LTBP3latent transforming growth factor beta binding protein 3 | Not recorded | In 1 condition |
| PHGDHphosphoglycerate dehydrogenase | Not recorded | In 1 condition |
| RNU4ATACRNA, U4atac small nuclear | Not recorded | In 1 condition |
| TAPT1transmembrane anterior posterior transformation 1 | Not recorded | In 1 condition |
| XRCC4X-ray repair cross complementing 4 | Not recorded | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
Narrower traits
Broader traits
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
AtlasWho We HelpOur ScienceProductsOutcomes
Log InAskSequence your genome↗
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks