Hypochondroplasia
id:
hypochondroplasia-320-13754567
title:
Hypochondroplasia
text:
Hypochondroplasia (HCH) is a developmental disorder caused by an autosomal dominant genetic defect in the fibroblast growth factor receptor 3 gene (FGFR3) that results in a disproportionately short stature, micromelia and a head that appears large in comparison with the underdeveloped portions of the body. It is classified as short-limbed dwarfism.
brand slug:
wiki
category slug:
encyclopedia
description:
Medical condition
original url:
https://en.wikipedia.org/wiki/Hypochondroplasia
date created:
date modified:
2023-10-27T14:29:29Z
main entity:
{"identifier":"Q1283054","url":"https://www.wikidata.org/entity/Q1283054"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/4/4e/Autosomal_dominant_-_en.svg","width":738,"height":1260}
fields total:
13
integrity:
15