Hypomelanosis of Ito (HMI)

Alias:
Incontinentia Pigmenti Achromians
Nevus of Ito
Nevus Fuscocaeruleus Acromiodeltoideus
Pigmentation Disorders
Incontinentia Pigmenti Achromians Syndrome
Incontinentia Pigmenti, Type I, Formerly
Skin Pigmentation Disorder
Bloch Sulzberger Syndrome
Bloch-Siemans Syndrome
Ito Hypomelanosis
Ip1, Formerly
Ito's Nevus
Hmi
Ipa
Ito
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Hypomelanosis of Ito, also known as incontinentia pigmenti achromians, is related to weber syndrome and rapidly involuting congenital hemangioma, and has symptoms including muscle spasticity, seizures and exanthema. An important gene associated with Hypomelanosis of Ito is GTF3C5 (General Transcription Factor IIIC Subunit 5), and among its related pathways/superpathways are Signal Transduction and Prolactin Signaling. The drugs Aldesleukin and Tacrolimus have been mentioned in the context of this disorder. Affiliated tissues include skin and eye, and related phenotypes are macrocephaly and intellectual disability
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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All ages
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16
136
41

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
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IF
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