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 64 for Abnormal relationship
  1. Crohn's disease 
    ... factors are probably related, directly or indirectly, to abnormal inflammation. However, the exact relationship between these factors and Crohn's disease risk ...
    https://medlineplus.gov/genetics/condition/crohns-disease - Genetics
  2. Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy 
    ... pain seen in people with CARASIL, although the relationship between abnormal TGF-β signaling and these features is less ...
    https://medlineplus.gov/...cortical-infarcts-and-leukoencephalopathy - Genetics
  3. COMP gene 
    ... Hecht JT, Vertel BM. COMP mutations: domain-dependent relationship between abnormal chondrocyte trafficking and clinical PSACH and MED phenotypes. ...
    https://medlineplus.gov/genetics/gene/comp - Genetics
  4. HTRA1 gene 
    ... pain seen in people with CARASIL, although the relationship between abnormal TGF-β signaling and these features is less ...
    https://medlineplus.gov/genetics/gene/htra1 - Genetics
  5. IDH2 gene 
    ... the production of D-2-hydroxyglutarate, but the relationship between the abnormal buildup of this substance and the signs and ...
    https://medlineplus.gov/genetics/gene/idh2 - Genetics
  6. DYRK1A gene 
    ... or absent DYRK1A enzyme function likely leads to abnormal regulation of gene expression and disrupts proper neural development. However, the specific relationship between DYRK1A gene mutations and the signs and ...
    https://medlineplus.gov/genetics/gene/dyrk1a - Genetics
  7. Infantile neuroaxonal dystrophy 
    ... neurons. In some individuals with infantile neuroaxonal dystrophy, abnormal amounts of iron accumulate in a specific region of the brain called the basal ganglia. The relationship of these features to the symptoms of infantile ...
    https://medlineplus.gov/.../infantile-neuroaxonal-dystrophy - Genetics
  8. SLC19A3 gene 
    ... basal ganglia, which help control movement, but the relationship between these specific brain abnormalities and the abnormal thiamine transporter is unknown. More About This Health ...
    https://medlineplus.gov/genetics/gene/slc19a3 - Genetics
  9. Biotin-thiamine-responsive basal ganglia disease 
    ... be seen, including in the basal ganglia. The relationship between these specific brain abnormalities and the abnormal thiamine transporter is unknown.It is unclear how ...
    https://medlineplus.gov/...thiamine-responsive-basal-ganglia-disease - Genetics
  10. Ollier disease 
    ... the respective gene to take on a new, abnormal function. Although these mutations have been found in some cells of enchondromas in people with Ollier disease, the relationship between the mutations and the signs and symptoms ...
    https://medlineplus.gov/genetics/condition/ollier-disease - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · next