Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 38 for child health human development
  1. HTT gene 
    ... As the gene is passed from parent to child, the size of the CAG trinucleotide repeat may lengthen into the range associated with Huntington's disease (36 repeats or more). More About This Health Condition HD HD_HUMAN huntingtin (Huntington disease) Huntington's disease protein IT15 ...
    https://medlineplus.gov/genetics/gene/htt - Genetics
  2. MTRR gene 
    ... associated with birth defects that occur during the development of the ... associated health problems. Researchers have not determined why there may ...
    https://medlineplus.gov/genetics/gene/mtrr - Genetics
  3. NSDHL gene 
    ... can contribute to problems with the growth and development of many parts of the body. It is not known, however, exactly how a disturbance in cholesterol synthesis leads to the specific features of CHILD syndrome. More About This Health Condition Variants in the NSDHL gene can cause ...
    https://medlineplus.gov/genetics/gene/nsdhl - Genetics
  4. FLT4 gene 
    ... and symptoms of Milroy disease. More About This Health Condition FLT41 fms-related tyrosine kinase 4 vascular endothelial growth factor receptor 3 VEGFR3 VGFR3_HUMAN Tests of FLT4 PubMed FMS-LIKE TYROSINE KINASE 4; FLT4 NCBI Gene ClinVar Brice G, Child AH, Evans A, Bell R, Mansour S, Burnand ...
    https://medlineplus.gov/genetics/gene/flt4 - Genetics
  5. TSEN54 gene 
    ... tRNA splicing endonuclease complex leads to abnormal brain development in people with pontocerebellar hypoplasia. More About This Health Condition FLJ37147 SEN54 SEN54_HUMAN SEN54L tRNA splicing endonuclease 54 homolog tRNA splicing ...
    https://medlineplus.gov/genetics/gene/tsen54 - Genetics
  6. MTR gene 
    ... risk of birth defects that occur during the development of the brain and ... and associated health problems, but other studies found no increased risk. ...
    https://medlineplus.gov/genetics/gene/mtr - Genetics
  7. FKRP gene 
    ... FKRP gene cause several different muscular dystrophies. FKRP_HUMAN LGMD2I MDC1C MDDGA5 MDDGB5 MDDGC5 Tests of FKRP PubMed FUKUTIN-RELATED PROTEIN; FKRP MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT), TYPE B, 5; MDDGB5 NCBI Gene ClinVar Beltran- ...
    https://medlineplus.gov/genetics/gene/fkrp - Genetics
  8. HPSE2 gene 
    ... 2 protein may lead to problems with the development of the urinary tract or with muscle function in the face and bladder. More About This Health Condition heparanase 2 heparanase-2 HPA2 HPR2 HPSE2_HUMAN Tests of HPSE2 PubMed HEPARANASE 2; HPSE2 NCBI ...
    https://medlineplus.gov/genetics/gene/hpse2 - Genetics
  9. LEP gene 
    ... involved in regulating the hormones that control sexual development. However, the specifics of this involvement and how it may be altered in congenital leptin deficiency are unknown. More About This Health Condition LEP_HUMAN LEPD leptin (murine obesity homolog) leptin (obesity homolog, ...
    https://medlineplus.gov/genetics/gene/lep - Genetics
  10. ALX4 gene 
    ... disability and distinctive facial features. More About This Health Condition ... C, Grochowsky A, Loukas M, Tubbs RS. Enlarged parietal foramina: a review of genetics, prognosis, radiology, and treatment. Childs Nerv Syst. 2013 Apr;29(4):543-7. ...
    https://medlineplus.gov/genetics/gene/alx4 - Genetics
previous · 1 · 2 · 3 · 4 · next