Entry - 173000 - PILONIDAL SINUS - OMIM

 
ICD+
173000

PILONIDAL SINUS


Clinical Synopsis
 

Skin
- Pilonidal sinus
Inheritance
- Autosomal dominant
▲ Close

▼ TEXT

Holmes and Turner (1969) observed 9 affected members in a family in a pattern consistent with autosomal dominant inheritance, although no male-to-male transmission was observed. However, father-son transmission was noted by Stone (1924).


▼ REFERENCES

  1. Holmes, L. B., Turner, E. A., Jr. Hereditary pilonidal sinus. JAMA 209: 1525-1526, 1969. [PubMed: 5820262, related citations]

  2. Stone, H. B. Pilonidal sinus (coccygeal fistula). Ann. Surg. 79: 410-414, 1924. [PubMed: 17864995, related citations]


Creation Date:
Victor A. McKusick : 6/2/1986
Edit History:
terry : 06/03/2009
mimadm : 1/14/1995
supermim : 3/16/1992
supermim : 3/20/1990
ddp : 10/27/1989
marie : 3/25/1988
reenie : 10/18/1986

173000

PILONIDAL SINUS


SNOMEDCT: 16225231000119104, 47639008;   ICD10CM: L05, L05.91;   ICD9CM: 685;  



TEXT

Holmes and Turner (1969) observed 9 affected members in a family in a pattern consistent with autosomal dominant inheritance, although no male-to-male transmission was observed. However, father-son transmission was noted by Stone (1924).


REFERENCES

  1. Holmes, L. B., Turner, E. A., Jr. Hereditary pilonidal sinus. JAMA 209: 1525-1526, 1969. [PubMed: 5820262]

  2. Stone, H. B. Pilonidal sinus (coccygeal fistula). Ann. Surg. 79: 410-414, 1924. [PubMed: 17864995]


Creation Date:
Victor A. McKusick : 6/2/1986

Edit History:
terry : 06/03/2009
mimadm : 1/14/1995
supermim : 3/16/1992
supermim : 3/20/1990
ddp : 10/27/1989
marie : 3/25/1988
reenie : 10/18/1986



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OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2024 Johns Hopkins University.

NOTE: OMIM is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced students in science and medicine. While the OMIM database is open to the public, users seeking information about a personal medical or genetic condition are urged to consult with a qualified physician for diagnosis and for answers to personal questions.
OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2024 Johns Hopkins University.
Printed: May 6, 2024