Skip to
  1. Homepage
  2. Rare diseases
  3. Search
Simple search

Simple search

*
(*) mandatory field





 

Other search option(s)

Isolated growth hormone deficiency type III

ORPHA231692
Synonym(s) Congenital IGHD type III
Congenital isolated GH deficiency type III
Congenital isolated growth hormone deficiency type III
X-linked IGHD
X-linked isolated growth hormone deficiency
Prevalence -
Inheritance X-linked recessive
Age of onset Neonatal
Infancy
ICD-10
  • E23.0
OMIM
UMLS -
MeSH -
MedDRA -

Summary

An Orphanet summary for this disease is currently under development. However, other data related to the disease are accessible from the Additional Information menu located on the right side of this page.


(*) Required fields.

Attention: Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. For all other comments, please send your remarks via contact us. Only comments written in English can be processed.


Captcha image
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.