Trait
Severe faltering weight
Clinical name: Severe failure to thrive
Summary
- Also called
- Severe weight faltering, Marked failure to thrive, Severe postnatal failure to thrive
- Body system
- Growth abnormality
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/severe-failure-to-thrive.json"
page <- fromJSON(url)
page$trait$nameRead the genes linked to Severe faltering weight, and the rest of your genome, with one test.
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Get my Genome Test16 genes linked to Severe faltering weight
Changes in these genes cause rare conditions in which Severe faltering weight 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 |
|---|---|---|
| LMNAlamin A/C | Very often (80–99%) | In 1 condition |
| ZMPSTE24zinc metallopeptidase STE24 | Very often (80–99%) | In 1 condition |
| ASXL1ASXL transcriptional regulator 1 | Often (30–79%) | In 1 condition |
| CPAPcentrosome assembly and centriole elongation protein | Often (30–79%) | In 1 condition |
| FIG4FIG4 phosphoinositide 5-phosphatase | Often (30–79%) | In 2 conditions |
| PRPS1phosphoribosyl pyrophosphate synthetase 1 | Often (30–79%) | In 1 condition |
| RTTNrotatin | Often (30–79%) | In 1 condition |
| VAC14VAC14 component of PIKFYVE complex | Often (30–79%) | In 1 condition |
| BSNDbarttin CLCNK type accessory subunit beta | Sometimes (5–29%) | In 1 condition |
| CLCNKAchloride voltage-gated channel Ka | Sometimes (5–29%) | In 1 condition |
| CLCNKBchloride voltage-gated channel Kb | Sometimes (5–29%) | In 1 condition |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Not recorded | In 1 condition |
| HYMAIhydatidiform mole associated and imprinted | Not recorded | In 1 condition |
| PEX7peroxisomal biogenesis factor 7 | Not recorded | In 1 condition |
| PLAGL1PLAG1 like zinc finger 1 | Not recorded | In 1 condition |
| ZFP57ZFP57 zinc finger protein | 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.
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.
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