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Results 1 - 10 of 953 for Parental
  1. Beckwith-Wiedemann syndrome 
    ... inherit one copy of this chromosome from each parent. For most genes on chromosome 11, both copies ... mother (the maternally inherited copy) is expressed. These parent-specific differences in gene expression are caused by ...
    https://medlineplus.gov/.../condition/beckwith-wiedemann-syndrome - Genetics
  2. Pseudoxanthoma elasticum 
    ... in each cell have mutations. Most often, the parents of an individual with an autosomal recessive condition ... few cases, an affected individual has one affected parent and one parent without the signs and symptoms ...
    https://medlineplus.gov/genetics/condition/pseudoxanthoma-elasticum - Genetics
  3. Genetic epilepsy with febrile seizures plus 
    ... affected person inherits the mutation from one affected parent. Other cases result from new (de novo) mutations ... mutations, although it can be inherited from a parent who has a milder form of GEFS+. Other ...
    https://medlineplus.gov/...netic-epilepsy-with-febrile-seizures-plus - Genetics
  4. Familial Mediterranean fever 
    ... MEFV gene in each cell have variants. The parents of an individual with an autosomal recessive condition ... individuals often inherit the variant from one affected parent.However, another mechanism is believed to account for ...
    https://medlineplus.gov/.../condition/familial-mediterranean-fever - Genetics
  5. 1q21.1 microdeletion 
    ... 1 microdeletion inherit the chromosomal change from a parent. In general, parents who carry a 1q21.1 microdeletion have milder ... the same size. About one-quarter of these parents have no associated features.A 1q21.1 microdeletion ...
    https://medlineplus.gov/genetics/condition/1q211-microdeletion - Genetics
  6. Central precocious puberty 
    ... of the gene (one copy inherited from each parent) are active in all cells. However, the activity of the MKRN3 gene depends on which parent it was inherited from. Only the copy inherited ...
    https://medlineplus.gov/.../condition/central-precocious-puberty - Genetics
  7. Familial hypercholesterolemia 
    ... altered copy of the gene from an affected parent and one normal copy of the gene from the other parent.Rarely, a person with familial hypercholesterolemia has a ...
    https://medlineplus.gov/.../condition/familial-hypercholesterolemia - Genetics
  8. Russell-Silver syndrome 
    ... s mother (the maternal copy) is expressed. These parent-specific differences in gene expression are caused by ... methylation is one way that a gene's parent of origin is marked during the formation of ...
    https://medlineplus.gov/genetics/condition/russell-silver-syndrome - Genetics
  9. Facioscapulohumeral muscular dystrophy 
    ... person inherits the altered chromosome from one affected parent. Other people with FSHD1 have no history of ... typically inherit the SMCHD1 gene mutation from one parent and the "permissive" chromosome 4 from the other ...
    https://medlineplus.gov/.../facioscapulohumeral-muscular-dystrophy - Genetics
  10. 15q11-q13 duplication syndrome 
    ... inherit one copy of chromosome 15 from each parent. However, some genes on this chromosome, including some ... on (active) only on the maternal copy. This parent-specific gene activation results from a phenomenon called ...
    https://medlineplus.gov/.../condition/15q11-q13-duplication-syndrome - Genetics
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