Orphanet: CLN5 disease

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CLN5 disease

ORPHA:228360

Classification level: Subtype of disorder

Synonym(s): -
Prevalence: -
Inheritance: Autosomal recessive
Age of onset: Childhood
ICD-10: E75.4
OMIM: 256731
UMLS: C1850442
MeSH: -
GARD: 1223
MedDRA: -

Summary

This disease is described under Late infantile neuronal ceroid lipofuscinosis

Detailed information

Professionals

Anesthesia guidelines
English (2016, pdf)

Review article
English (2016)

Clinical genetics review
English (2013)

Additional information

Further information on this disease

Health care resources for this disease

Research activities on this disease

Specialised Social Services

Eurordis directory

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.