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Results 1 - 10 of 250 for slow
  1. PRPH2 gene 
    ... by PRPH2 gene mutations, retinitis pigmentosa involves a slow degeneration of photoreceptor cells, leading to progressive vision ... of retinal abnormalities. CACD2 peripherin 2 (retinal degeneration, slow) peripherin 2, homolog of mouse peripherin, photoreceptor type ...
    https://medlineplus.gov/genetics/gene/prph2 - Genetics
  2. ATP2A2 gene 
    ... Health Condition AT2A2_HUMAN ATP2B ATPase, Ca++ dependent, slow-twitch, cardiac muscle-2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 calcium-transporting ATPase sarcoplasmic reticulum type, ...
    https://medlineplus.gov/genetics/gene/atp2a2 - Genetics
  3. TPM3 gene 
    ... gene provides instructions for making a protein called slow muscle alpha (α)-tropomyosin, which is part of ... proteins play a role in controlling cell shape.Slow muscle α-tropomyosin is found in skeletal muscles, ...
    https://medlineplus.gov/genetics/gene/tpm3 - Genetics
  4. Epilepsy-aphasia spectrum 
    ... the brain called continuous spike and waves during slow-wave sleep (CSWS). This pattern occurs while the affected child is sleeping, specifically during deep (slow-wave) sleep.Most children with LKS develop normally ...
    https://medlineplus.gov/genetics/condition/epilepsy-aphasia-spectrum - Genetics
  5. MYH7 gene 
    ... Type I fibers, which are also known as slow-twitch fibers, are one of two types of ... MGC138376 MGC138378 MPD1 MYH7_HUMAN MyHC-beta myhc-slow MYHCB myosin heavy chain (AA 1-96) Myosin ...
    https://medlineplus.gov/genetics/gene/myh7 - Genetics
  6. Perry syndrome 
    ... as parkinsonism, psychiatric changes, weight loss, and abnormally slow breathing (hypoventilation). These signs and symptoms typically appear ... of Perry syndrome. Signs of parkinsonism include unusually slow movements (bradykinesia), stiffness, and tremors. These movement abnormalities ...
    https://medlineplus.gov/genetics/condition/perry-syndrome - Genetics
  7. GRIN2A gene 
    ... also appear to play a role during deep (slow-wave) sleep.The GluN2A subunit of NMDA receptors ... abnormal electrical activity in the brain, usually during slow-wave sleep; a loss of speech and language ...
    https://medlineplus.gov/genetics/gene/grin2a - Genetics
  8. Russell-Silver syndrome 
    ... Silver syndrome is a growth disorder characterized by slow growth before and after birth. Babies with this ... the regulation of these genes, which leads to slow growth and the other characteristic features of this ...
    https://medlineplus.gov/genetics/condition/russell-silver-syndrome - Genetics
  9. Von Willebrand disease 
    Von Willebrand disease is a bleeding disorder that slows the blood clotting process, causing prolonged bleeding after ... is available, blood clots cannot form properly. Abnormally slow blood clotting causes the prolonged bleeding episodes seen ...
    https://medlineplus.gov/genetics/condition/von-willebrand-disease - Genetics
  10. KCNE1 gene 
    ... delayed rectifier potassium channel subunit IsK IKs producing slow voltage-gated potassium channel beta subunit Mink ISK ...
    https://medlineplus.gov/genetics/gene/kcne1 - Genetics
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