Overview
Clinical overview and emergency guidance are pending physician authorship. Graph-derived data (ontology codes, linked conditions, diagnostic biomarkers) is available below.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Biotinidase deficiency
Frequent (30-79%)
African trypanosomiasis
Frequent (30-79%)
Leigh's disease
Frequent (30-79%)
Adrenoleukodystrophy
Frequent (30-79%)
Gerstmann-Straussler-Scheinker syndrome
Frequent (30-79%)
Sotos' syndrome
Frequent (30-79%)
Trypanosomiasis
Frequent (30-79%)
Sanfilippo syndrome
Frequent (30-79%)
Prader-Willi syndrome
Frequent (30-79%)
Doose syndrome
Occasional (5-29%)
Acute intermittent porphyria
Occasional (5-29%)
GM1 gangliosidosis
Very frequent (80-99%)
Wolcott-Rallison dysplasia
Occasional (5-29%)
Spondyloenchondrodysplasia
Frequent (30-79%)
Free-living amoeba infection
Frequent (30-79%)
Spondyloenchondromatosis
Frequent (30-79%)
Vanishing white matter disease
Very frequent (80-99%)
Reversible cerebral vasoconstriction syndrome
Frequent (30-79%)
Legius syndrome
Very rare (1-4%)
ALG12-congenital disorder of glycosylation
Occasional (5-29%)
Neurogenic arthrogryposis multiplex congenita
Occasional (5-29%)
Proximal 16p11.2 microdeletion syndrome
Frequent (30-79%)
Asparagine-linked glycosylation 1 congenital disorder of glycosylation
Frequent (30-79%)
Congenital disorder of glycosylation type 1j
Occasional (5-29%)
Isolated focal cortical dysplasia
Very frequent (80-99%)
Quick Facts
- SNOMED CT
- 442731005
- UMLS CUI
- C2711610
- Fully Specified Name
- Imaging of brain abnormal (finding)
- Associated Conditions
- 25
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.