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Toe, misshapen

MedGen UID:
396052
•Concept ID:
C1861061
•
Finding
Synonym: TOE, MISSHAPEN
 
Monarch Initiative: MONDO:0008577
OMIM®: 189100

Clinical features

From HPO
Abnormality of the skeletal system
MedGen UID:
867418
•Concept ID:
C4021790
•
Anatomical Abnormality
An abnormality of the skeletal system.
See: Feature record | Search on this feature

Recent clinical studies

Etiology

A novel XK gene mutation in a Taiwanese family with McLeod syndrome.
Chen PY, Lai SC, Yang CC, Lee MJ, Chiu YH, Yan SH, Lu CS, Yeh TH
J Neurol Sci 2014 May 15;340(1-2):221-4. Epub 2014 Feb 27 doi: 10.1016/j.jns.2014.02.027. PMID: 24635891

Diagnosis

A novel XK gene mutation in a Taiwanese family with McLeod syndrome.
Chen PY, Lai SC, Yang CC, Lee MJ, Chiu YH, Yan SH, Lu CS, Yeh TH
J Neurol Sci 2014 May 15;340(1-2):221-4. Epub 2014 Feb 27 doi: 10.1016/j.jns.2014.02.027. PMID: 24635891

Supplemental Content

Table of contents

    Clinical resources

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    Related information

    • OMIM
      Related records in OMIM
    • PubMed
      Related literature resources in PubMed
    • PubMed (OMIM)
      Related literature resources in PubMed

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