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X-linked agammaglobulinemia with growth hormone deficiency

disorder
SNOMED 234533006CUI C0472813

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

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

Decreased body height
Always present (100%)HP:0004322
Delayed puberty
Always present (100%)HP:0000823
Delayed skeletal development
Always present (100%)HP:0002750
Absent circulating B cells
Frequent (30-79%)HP:0030252
Decreased response to growth hormone stimulation test
Frequent (30-79%)HP:0000824
Panypogammaglobulinemia
Frequent (30-79%)HP:0003139
Pink eye
Frequent (30-79%)HP:0000509
Recurrent middle ear infection
Frequent (30-79%)HP:0000403
Abnormal number of T cells
Excluded (<1%)HP:0011839
Brain inflammation
HP:0002383
Deafness
HP:0000365
Diarrhea
HP:0002014
Enteroviral dermatomyositis syndrome
HP:0003729
Enteroviral hepatitis
HP:0001412
Epididymitis
HP:0000031
Meningitis
HP:0001287
Pneumonia
HP:0002090
Prostatitis
HP:0000024
Pyoderma
HP:0000999
Recurrent bacterial infections
HP:0002718
Recurrent enteroviral infections
HP:0002743
Repeated bladder infections
HP:0000010
Septic arthritis
HP:0003095
Sinus disease
HP:0000246

Quick Facts

SNOMED CT
234533006
UMLS CUI
C0472813
Fully Specified Name
X-linked agammaglobulinemia with growth hormone deficiency (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.