Skip to main content

RareConnect.ioRare Intelligence

Explore Data Discover Patient Groups News Partner

Sign In Sign Up

Explore Data Patient Groups News Partner

RareConnect.ioRare Intelligence

Combining the speed of AI with the wisdom of the community to build the world's most accurate disease registry.

Explore

Disease Directory
Patient Groups
News
FAQ
MONDO Ontology ↗

Get Involved

Partner with Us
Register Your PAG
Community
Pricing

Legal

Privacy Policy
Terms of Service
Accessibility
Contact Us

© 2025 RareConnect.io. Powered by MONDO Ontology

wooly hair, autosomal recessive 3 | RareConnect | RareConnect.io

/hereditary disease

/isolated familial wooly hair disorder

/wooly hair, autosomal recessive 3

wooly hair, autosomal recessive 3

Rare Disease

MONDO:0014765

Also Known As

ARWH3KRT25 woolly hair (disease)KRT25 wooly hair (disease)woolly hair (disease) caused by mutation in KRT25woolly hair, autosomal recessive type 3wooly hair (disease) caused by mutation in KRT25wooly hair, autosomal recessive 3wooly hair, autosomal recessive type 3woolly hair, autosomal recessive 3, with hypotrichosiswooly hair, autosomal recessive 3, with hypotrichosis

Definition

Any wooly hair in which the cause of the disease is a mutation in the KRT25 gene.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

Checking for content...

Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:616760 ↗

GARD

Related Diseases

inherited bleeding disorder, platelet-type

MONDO:0000009

infantile liver failure

MONDO:0000023

febrile seizures, familial

MONDO:0000032

hereditary hypophosphatemic rickets

MONDO:0000044

hypothyroidism, congenital, nongoitrous

MONDO:0000045

isolated microphthalmia

MONDO:0000062

← Back to All Diseases