WHIM - Warts, hypogammaglobulinaemia, infections and myelokathexis

disorder

SNOMED 234571003CUI C0472817

Overview

WHIM - Warts, hypogammaglobulinaemia, infections and myelokathexis 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 neutrophil morphology

Very frequent (80-99%)HP:0011992

Absolute lymphocyte count decrease

Very frequent (80-99%)HP:0001888

Bone marrow hypercellularity

Very frequent (80-99%)HP:0031020

Neutropoenia

Very frequent (80-99%)HP:0001875

Decreased circulating immunoglobulin concentration

Frequent (30-79%)HP:0004313

Papilloma

Frequent (30-79%)HP:0012740

Pneumonia

Frequent (30-79%)HP:0002090

Prone to bacterial infection

Frequent (30-79%)HP:0002718

pulmonary infections, recurrent

Frequent (30-79%)HP:0006532

Recurrent URI

Frequent (30-79%)HP:0002788

Respiratory infection

Frequent (30-79%)HP:0011947

Warts

Frequent (30-79%)HP:0200043

Abnormal vocalization

Occasional (5-29%)HP:0002167

Abnormality of the small intestine

Occasional (5-29%)HP:0002244

Appendicular ataxia

Occasional (5-29%)HP:0002070

Bronchiectasis

Occasional (5-29%)HP:0002110

Cervix cancer

Occasional (5-29%)HP:0030079

Fine motor skill dysfunction

Occasional (5-29%)HP:0007010

Otitis media

Occasional (5-29%)HP:0000388

Pharyngitis

Occasional (5-29%)HP:0025439

Postural instability

Occasional (5-29%)HP:0002172

Sinus disease

Occasional (5-29%)HP:0000246

Tetrology of fallot

Occasional (5-29%)HP:0001636

Blotchy loss of skin colour

Very rare (1-4%)HP:0001045

Cutaneous melanoma

Very rare (1-4%)HP:0012056

Infection in blood stream

Very rare (1-4%)HP:0100806

Inflammation of the lymph nodes

Very rare (1-4%)HP:0002840

Meningitis

Very rare (1-4%)HP:0001287

Parotitis

Very rare (1-4%)HP:0011850

Pulmonary atelectasis

Very rare (1-4%)HP:0100750

Related Conditions

Severe combined immunodeficiency disease(parent)

Disorder of immune structure(parent)

Myelokathexis(parent)

Hereditary white blood cell disorder(parent)

Congenital neutropenia(parent)

Quick Facts

SNOMED CT: 234571003
UMLS CUI: C0472817
Fully Specified Name: Warts, hypogammaglobulinemia, infections, and myelokathexis (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.