Hepatic veno-occlusive disease with immunodeficiency syndrome

disorder

SNOMED 724361001CUI C4510630

Overview

Hepatic veno-occlusive disease with immunodeficiency 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.

Abnormal circulating interferon-gamma concentration

Very frequent (80-99%)HP:0030355

Abnormal number of lymphocytes

Very frequent (80-99%)HP:0040088

Abnormality of interleukin secretion

Very frequent (80-99%)HP:0011117

Panypogammaglobulinemia

Very frequent (80-99%)HP:0003139

Coughing

Frequent (30-79%)HP:0012735

Decreased proportion of memory B cells

Frequent (30-79%)HP:0030374

Enlarged liver

Frequent (30-79%)HP:0002240

Failure to thrive in first year of life

Frequent (30-79%)HP:0001531

Hepatosplenomegaly

Frequent (30-79%)HP:0001433

Lymph nodes lack germinal center

Frequent (30-79%)HP:0002849

Recurrent enteroviral infections

Frequent (30-79%)HP:0002743

Recurrent gastroenteritis

Frequent (30-79%)HP:0031123

Recurrent viral infections

Frequent (30-79%)HP:0004429

Reduced number of T cells

Frequent (30-79%)HP:0005403

respiratory infections, recurrent

Frequent (30-79%)HP:0002205

Ascites

Occasional (5-29%)HP:0001541

Chronic hepatic failure

Occasional (5-29%)HP:0100626

Diarrhea

Occasional (5-29%)HP:0002014

Generalized tonic-clonic seizure (without specification of onset)

Occasional (5-29%)HP:0002069

Hemiparesis

Occasional (5-29%)HP:0001269

Inappropriate antidiuretic hormone secretion

Occasional (5-29%)HP:0031218

Intrapulmonary hemorrhage

Occasional (5-29%)HP:0040223

Leg paralysis

Occasional (5-29%)HP:0010550

Leukodystrophy

Occasional (5-29%)HP:0002415

Low number of red blood cells or hemoglobin

Occasional (5-29%)HP:0001903

Mucocutaneous candidiasis

Occasional (5-29%)HP:0002728

Pancytopenia

Occasional (5-29%)HP:0001876

Partial paralysis of legs

Occasional (5-29%)HP:0002385

Portal hypertension

Occasional (5-29%)HP:0001409

Pulmonary fibrosis

Occasional (5-29%)HP:0002206

Related Conditions

Veno-occlusive disease of the liver(parent)

Autosomal recessive severe combined immunodeficiency disease(parent)

Cardiovascular system hereditary disorder(parent)

Digestive system hereditary disorder(parent)

Severe combined immunodeficiency with low T- and B-cell numbers(parent)

Disorder of digestive system specific to fetus OR newborn(parent)

Quick Facts

SNOMED CT: 724361001
UMLS CUI: C4510630
Fully Specified Name: Hepatic veno-occlusive disease with immunodeficiency syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 30

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.