Warning: The NCBI web site requires JavaScript to function. more...

Full Report

Format

Full Report
Summary (Text)
Summary (XML)

Send to:

Choose Destination

File
Clipboard
Collections

Modifier, X-linked, for Neurofunctional defects

MedGen UID:: 326945
•Concept ID:: C1839708
•: Disease or Syndrome

Synonym:	TOURETTE SYNDROME, MODIFIER OF

Monarch Initiative:	MONDO:0010673
OMIM®:	309840

Clinical features

From HPO

Abnormality of the nervous system

MedGen UID:: 105425
•Concept ID:: C0497552
•: Congenital Abnormality

An abnormality of the nervous system.

See: Feature record | Search on this feature

Abnormality of the nervous system
- Abnormality of the nervous system

Supplemental Content

Table of contents

Clinical resources

Molecular resources

Coriell Institute for Medical Research

Consumer resources

Reviews

Related information

MeSH
Related Medical Subject Headings
OMIM
Related records in OMIM
PMC Articles
Related information in PubMed Central Links
PubMed
Related literature resources in PubMed

Recent activity

Clear Turn Off Turn On

Modifier, X-linked, for Neurofunctional defects
Modifier, X-linked, for Neurofunctional defects

MedGen
Pvrig poliovirus receptor related immunoglobulin domain containing [Mus musculus...
Pvrig poliovirus receptor related immunoglobulin domain containing [Mus musculus]
Gene ID:102640920

Gene
Abnormal mitral valve morphology
Abnormal mitral valve morphology

MedGen
Visual halos
Visual halos

MedGen
Post-traumatic coma
Post-traumatic coma

MedGen

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...