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Marcus Gunn phenomenon (CUI C0266521) Suggest changes to this concept
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Terms & Properties

Concept Unique Identifier (CUI): C0266521

Semantic Type: Disease or Syndrome

GARD Definition: Marcus Gunn phenomenon is a rare condition characterized by movement of the upper eyelid in a rapid rising motion (a "wink") each time the jaw moves. The wink phenomenon may be elicited by opening the mouth, thrusting the jaw to the side, jaw protrusion, chewing, smiling, or sucking. It is usually present at birth and may occur with other eye abnormalities (such as strabismus) or vision problems. t can affect both eyes in rare cases. The exact cause is not known. Marcus Gunn phenomenon is generally sporadic, but familial cases with autosomal dominant inheritance have been reported. Treatment is not always needed but may include surgery in more severe cases. - this information is from GARD/ORDR/NCATS.

Synonyms & Abbreviations: (see Synonym Details)
Abnorm innervation synd
Abnormal eyelid innervation syndrome
Abnormal innervation syndrome of eyelid
Familial Marcus Gunn phenomenon (subtype)
Familial Marcus Gunn phenomenon
Jaw blinking
Jaw winking
Jaw-blinking (disorder)
Jaw-blinking
Jaw-winking syndrome (disorder)
Jaw-winking syndrome
Jaw-winking
Mandibulo-palpebral synkinesis - ptosis
Marcus Gunn phenomenon
Marcus Gunn phenonemon
Marcus Gunn syndrome
Marcus Gunn's syndrome
Marcus-Gunn jaw winking
Marcus-Gunn phenomenon
Marcus-Gunn syndrome
Maxillopalpebral synkinesis
Pterygoid-levator synkinesis

External Source Codes:  (none)

Other Properties: Property Definitions
Name Value Source
ACTIVE 1 SNOMEDCT_US
CASE_SIGNIFICANCE_ID 900000000000017005 SNOMEDCT_US
CASE_SIGNIFICANCE_ID 900000000000020002 SNOMEDCT_US
CTV3ID XUCbc SNOMEDCT_US
CTV3ID XUFZG SNOMEDCT_US
DATE_CREATED 2013-01-09T00:04:00 GARD
DATE_CREATED 2015-01-22T00:04:00 GARD
DATE_LAST_MODIFIED 2013-01-09T00:04:00 GARD
DEFINITION_STATUS_ID 900000000000074008 SNOMEDCT_US
DISEASE_IDENTIFIER_ID 34475 GARD
DISEASE_IDENTIFIER_ID 34476 GARD
DISEASE_IDENTIFIER_ID 34477 GARD
DISEASE_IDENTIFIER_ID 34478 GARD
DISEASE_IDENTIFIER_ID 4660 GARD
DISEASE_IDENTIFIER_ID 4661 GARD
DISEASE_IDENTIFIER_ID 4662 GARD
DISEASE_IDENTIFIER_ID 4663 GARD
EFFECTIVE_TIME 20020131 SNOMEDCT_US
FR 59 MSH
HAS_GARD_PAGE true GARD
HM D001763 MSH
HM D006330 MSH
HM D007569 MSH
HM D009422 MSH
HM D012021 MSH
ICE Jaw-blinking; Paradoxical facial movements ICD9CM
IDENTIFIER_SOURCE Orp GARD
IDENTIFIER_TYPE_ID 1 GARD
IS_ACTIVE true GARD
IS_RARE true GARD
IS_SPANISH false GARD
LAST_REVIEW_DATE 2007-04-23T00:00:00 GARD
MDA 20100825 MSH
MIMTYPE 0 OMIM
MIMTYPEMEANING Other, mainly phenotypes with suspected mendelian basis OMIM
MIMTYPEVALUE none OMIM
MMR 20150818 MSH
PRIMARY_PATH 10064583$10015984$10015920$10010331$Marcus Gunn syndrome$Eyelid disorders congenital$Eye disorders congenital$Congenital, familial and genetic disorders MDR
PRIMARY_SOC 10010331 MDR
PT_IN_VERSION 10.0 MDR
PT_IN_VERSION 10.1 MDR
PT_IN_VERSION 11.0 MDR
PT_IN_VERSION 11.1 MDR
PT_IN_VERSION 12.0 MDR
PT_IN_VERSION 12.1 MDR
PT_IN_VERSION 13.0 MDR
PT_IN_VERSION 13.1 MDR
PT_IN_VERSION 14.0 MDR
PT_IN_VERSION 14.1 MDR
PT_IN_VERSION 15.0 MDR
PT_IN_VERSION 15.1 MDR
PT_IN_VERSION 16.0 MDR
PT_IN_VERSION 16.1 MDR
PT_IN_VERSION 17.0 MDR
PT_IN_VERSION 17.1 MDR
PT_IN_VERSION 18.0 MDR
PT_IN_VERSION 18.1 MDR
PT_IN_VERSION 19.0 MDR
PT_IN_VERSION 19.1 MDR
PT_IN_VERSION 8.1 MDR
PT_IN_VERSION 9.0 MDR
PT_IN_VERSION 9.1 MDR
RARE_DISEASE_URL http://rarediseases.info.nih.gov/gard/6972/marcus-gunn-phenomenon/resources/1 GARD
RN 0 MSH
SC 3 MSH
SMQ_TERM_ADDVERSION 10.0 MDR
SMQ_TERM_ADDVERSION 12.1 MDR
SMQ_TERM_CAT A MDR
SMQ_TERM_LEVEL 4 MDR
SMQ_TERM_LEVEL 5 MDR
SMQ_TERM_LMVERSION 12.1 MDR
SMQ_TERM_LMVERSION 14.0 MDR
SMQ_TERM_SCOPE 2 MDR
SMQ_TERM_STATUS A MDR
SMQ_TERM_WEIGHT 0 MDR
SNOMEDID D4-96310 SNOMEDCT_US
SNOMEDID DA-76401 SNOMEDCT_US
SOS A rare condition of unknown etiology that is characterized by movement of the upper eyelid in a rapid rising motion (a "wink") each time the jaw moves. This phenomenon may be elicited by opening the mouth, thrusting the jaw to the side, jaw protrusion, chewing, smiling, or sucking. It is usually present at birth and may occur with other eye abnormalities (such as STRABISMUS) or vision problems. It is usually unilateral but can affect both eyes in rare cases. It is generally sporadic, but familial cases with autosomal dominant inheritance have been reported. OMIM: 154600 MSH
SUBSET_MEMBER 447562003~CORRELATIONID~447561005 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPADVICE~ALWAYS Q07.8 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPCATEGORYID~447637006 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPGROUP~1 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPPRIORITY~1 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPRULE~TRUE SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPTARGET~Q07.8 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~CORRELATIONID~447561005 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~ALWAYS H02.519 | CONSIDER LATERALITY SPECIFICATION SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~ALWAYS Q07.8 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPCATEGORYID~447637006 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPGROUP~1 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPPRIORITY~1 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPRULE~TRUE SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPTARGET~H02.519 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPTARGET~Q07.8 SNOMEDCT_US
SUBSET_MEMBER 900000000000497000~MAPTARGET~XUCbc SNOMEDCT_US
SUBSET_MEMBER 900000000000497000~MAPTARGET~XUFZG SNOMEDCT_US
SUBSET_MEMBER 900000000000498005~MAPTARGET~D4-96310 SNOMEDCT_US
SUBSET_MEMBER 900000000000498005~MAPTARGET~DA-76401 SNOMEDCT_US
SUBSET_MEMBER 900000000000508004~ACCEPTABILITYID~900000000000548007 SNOMEDCT_US
SUBSET_MEMBER 900000000000508004~ACCEPTABILITYID~900000000000549004 SNOMEDCT_US
SUBSET_MEMBER 900000000000509007~ACCEPTABILITYID~900000000000548007 SNOMEDCT_US
SUBSET_MEMBER 900000000000509007~ACCEPTABILITYID~900000000000549004 SNOMEDCT_US
TERMUI T737627 MSH
TERMUI T737628 MSH
TERMUI T737629 MSH
TERMUI T753777 MSH
TH OMIM (2013) MSH
TH ORD (2010) MSH
TYPE_ID 900000000000003001 SNOMEDCT_US
TYPE_ID 900000000000013009 SNOMEDCT_US

Additional Concept Data:  (none)

URL to Bookmark: https://ncim-stage.nci.nih.gov/ncimbrowser/ConceptReport.jsp?dictionary=NCI Metathesaurus&code=C0266521

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