Keratosis Follicularis Spinulosa Decalvans

Alias:
Keratosis Follicularis Spinulosa Decalvans, Autosomal Dominant
Keratosis Follicularis Spinulosa Decalvans, X-Linked
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Keratosis Follicularis Spinulosa Decalvans, also known as keratosis follicularis spinulosa decalvans, autosomal dominant, is related to keratosis follicularis spinulosa decalvans, x-linked and keratosis, and has symptoms including photophobia An important gene associated with Keratosis Follicularis Spinulosa Decalvans is MBTPS2 (Membrane Bound Transcription Factor Peptidase, Site 2), and among its related pathways/superpathways are Metabolism and Regulation of expression of SLITs and ROBOs. Affiliated tissues include skin and bone.
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
XLD
AD
AR
XL
Child
--
26
130
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Medical Symptom

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Gene & Mutation

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Related Drugs

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No data available

Disease Model

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MGI
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References Literature

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