Overview
Zaki Gleeson 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.
5th finger camptodactyly
HP:0009183
Bradycardia
HP:0001662
Cortical gyral simplification
HP:0009879
Cortical white matter abnormalities seen on MRI
HP:0002500
Decreased size of cranium
HP:0000252
Dystonic disease
HP:0001332
Full lower lip
HP:0000179
Generalised decreased muscle tone
HP:0001290
Glucose intolerance
HP:0001952
Glucose tolerance decreased
HP:0040270
Hyperplasia of nose
HP:0000448
Hypoplasia of corpus callosum
HP:0002079
Increased horizontal length of eyebrow
HP:0004523
Increased length of philtrum
HP:0000343
Increased reflexes
HP:0001347
Increased width of the forehead
HP:0000337
Instability or lack of coordination of central trunk muscles
HP:0002078
Interruption of electrical communication between upper and lower chambers of heart
HP:0001678
IQ less than 20
HP:0002187
Large ears
HP:0000400
Long fingers
HP:0100807
Microcephaly, progressive
HP:0000253
Muscular hypotonia
HP:0001252
No speech development
HP:0001344
Permanent curving of the pinkie finger
HP:0004209
Persistent blue colour of hands or feet
HP:0001063
Poor weight gain
HP:0001508
Prominent antihelix
HP:0000395
Retarded growth
HP:0001510
Small cerebellum
HP:0001321
Related Conditions
Congenital cerebellar hypoplasia(parent)
Multiple malformation syndrome with facial-limb defects as major feature(parent)
Recessive hereditary disorder (autosomal)(parent)
Congenital conduction defect(parent)
Cardiovascular system hereditary disorder(parent)
Hereditary disorder of nervous system(parent)
Developmental hereditary disorder(parent)
Congenital microcephalus(parent)
Genetic intellectual disability(parent)
Quick Facts
- SNOMED CT
- 764732004
- UMLS CUI
- C3280692
- Fully Specified Name
- Microcephalus, cerebellar hypoplasia, cardiac conduction defect 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.