Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome

disorder

SNOMED 733028000CUI C4518551

Overview

Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome 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.

Abnormality of coagulation

Very frequent (80-99%)HP:0001928

Abnormality of leukocytes

Very frequent (80-99%)HP:0001881

Ataxia

Very frequent (80-99%)HP:0001251

Corticospinal signs

Very frequent (80-99%)HP:0007256

Dizziness

Very frequent (80-99%)HP:0002321

Double vision

Very frequent (80-99%)HP:0000651

Gait disturbance

Very frequent (80-99%)HP:0001288

Ichthyosiform abnormality of the skin

Very frequent (80-99%)HP:0008064

Optic atrophy

Very frequent (80-99%)HP:0000648

Retrobulbar neuritis

Very frequent (80-99%)HP:0100654

Sensory neuropathy

Very frequent (80-99%)HP:0000763

Paralysis or weakness of one side of body

Frequent (30-79%)HP:0004374

Related Conditions

Hereditary coagulation factor deficiency(parent)

Multiple sclerosis(parent)

Lamellar ichthyosis(parent)

Congenital anomaly of central nervous system(parent)

Hereditary disorder of immune system(parent)

Congenital degeneration of nervous system(parent)

Hereditary degenerative disease of central nervous system(parent)

Chronic skin disease(parent)

Quick Facts

SNOMED CT: 733028000
UMLS CUI: C4518551
Fully Specified Name: Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 12

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.