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HMI - Hypomelanosis of Ito

disorder
SNOMED 218358001CUI C0022283

Overview

HMI - Hypomelanosis of Ito is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Naevi
Very frequent (80-99%)HP:0003764
Cutaneous melanoma
Very rare (1-4%)HP:0012056
Cerebral atrophy
HP:0002059
Coarse face
HP:0000280
Cobb angle greater than ten degrees
HP:0002650
Curvature of digit
HP:0030084
Decreased size of cranium
HP:0000252
Dull intelligence
HP:0001249
Full lower lip
HP:0000179
Gray matter heterotopias
HP:0002282
Hair loss
HP:0001596
Hunched back
HP:0002808
Increased distance between eyes
HP:0000316
Increased size of skull
HP:0000256
Iris coloboma
HP:0000612
Lens opacities
HP:0000518
Macular hypopigmented whorls, streaks, and patches
HP:0005593
Palpebronasal fold
HP:0000286
Polydactyly of the hand
HP:0001161
Radial deviation of finger
HP:0009466
Seizures
HP:0001250
Squint
HP:0000486
Syndactyly
HP:0001159
Variability of spacing between teeth
HP:0006316

Related Conditions

Quick Facts

SNOMED CT
218358001
UMLS CUI
C0022283
Fully Specified Name
Incontinentia pigmenti achromians syndrome (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
24
Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.