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 - 8 of 8 for Nasal disorder
  1. FREM1 gene 
    ... membranes of particular tissues, resulting in the cleft nasal cartilage (bifid nose), missing kidneys (renal agenesis), narrowed or misplaced anal opening (anorectal malformations), and other features characteristic of this disorder. Researchers suggest that BNAR and Manitoba oculotrichoanal syndrome, ...
    https://medlineplus.gov/genetics/gene/frem1 - Genetics
  2. TXNL4A gene 
    ... identified in people with Burn-McKeown syndrome, a disorder that is present from birth (congenital) and involves abnormalities of the nasal passages, characteristic facial features, hearing loss, heart abnormalities, ...
    https://medlineplus.gov/genetics/gene/txnl4a - Genetics
  3. SMCHD1 gene 
    ... development of the head and face. Problems with nasal development may affect ... a disorder characterized by muscle weakness and wasting (atrophy) that ...
    https://medlineplus.gov/genetics/gene/smchd1 - Genetics
  4. KIT gene 
    ... another blood cell cancer that occurs in the nasal passages. In addition, some people with seminoma, a type of ... D, Katsambas AD. A review of genetic disorders of hypopigmentation: lessons learned from the biology of ...
    https://medlineplus.gov/genetics/gene/kit - Genetics
  5. SPECC1L gene 
    ... cells that come together to form the forehead, nasal bridge, and lower jaw. ... About This Health Condition Mutations in the ...
    https://medlineplus.gov/genetics/gene/specc1l - Genetics
  6. SCN9A gene 
    ... sensory neurons, which are nerve cells in the nasal cavity that transmit ... extreme pain disorder. This condition is characterized by severe pain attacks ...
    https://medlineplus.gov/genetics/gene/scn9a - Genetics
  7. SLC3A1 gene 
    ... with a prominent forehead, long eyelashes, a flat nasal bridge, and abnormally turned ears. ... G, Creemers JW. Multi-system disorder syndromes associated with cystinuria type I. Curr Mol ...
    https://medlineplus.gov/genetics/gene/slc3a1 - Genetics
  8. ALX4 gene 
    ... it is unclear whether these conditions are distinct disorders or part of a disease spectrum. ... S, Uyguner ZO. Mild nasal malformations and parietal foramina caused by homozygous ALX4 ...
    https://medlineplus.gov/genetics/gene/alx4 - Genetics