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Malan overgrowth syndrome

disorder
SNOMED 763795006CUI C3553660

Overview

Malan overgrowth 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.

Dull intelligence
Always present (100%)HP:0001249
General overgrowth
Always present (100%)HP:0001548
Speech and language difficulties
Always present (100%)HP:0000750
Early bone maturation
Very frequent (80-99%)HP:0005616
Peripheral hypotonia
Very frequent (80-99%)HP:0001252
Vertical enlargement of face
Very frequent (80-99%)HP:0000276
Abnormal curving of the cornea or lens of the eye
Frequent (30-79%)HP:0000483
Accelerated linear growth
Frequent (30-79%)HP:0000098
ASD
Frequent (30-79%)HP:0000729
Bulging forehead
Frequent (30-79%)HP:0011220
Coxa valga deformity
Frequent (30-79%)HP:0002673
Cutis marmorata
Frequent (30-79%)HP:0000965
Decreased projection of midface
Frequent (30-79%)HP:0011800
Dilated cerebral ventricle
Frequent (30-79%)HP:0002119
Down-slanting palpebral fissure
Frequent (30-79%)HP:0000494
Eclabium of lower lip
Frequent (30-79%)HP:0000232
Feeding difficulties in infancy
Frequent (30-79%)HP:0008872
Gum enlargement
Frequent (30-79%)HP:0000212
High forehead
Frequent (30-79%)HP:0000348
Hyperopia
Frequent (30-79%)HP:0000540
Hypoplasia of corpus callosum
Frequent (30-79%)HP:0002079
Hypotonia, in neonatal onset
Frequent (30-79%)HP:0001319
Increased size of skull
Frequent (30-79%)HP:0000256
Long fingers
Frequent (30-79%)HP:0100807
Low posterior hair line
Frequent (30-79%)HP:0002162
Mandibular excess
Frequent (30-79%)HP:0000303
Moderate mental retardation
Frequent (30-79%)HP:0002342
No development of motor milestones
Frequent (30-79%)HP:0001270
Oval facies
Frequent (30-79%)HP:0000300
Pectus excavatum
Frequent (30-79%)HP:0000767

Related Conditions

Multiple malformation syndrome with early overgrowth(parent)
Multiple malformation syndrome with facial defects as major feature(parent)
Developmental hereditary disorder(parent)
Congenital macrocephaly(parent)
Genetic intellectual disability(parent)

Quick Facts

SNOMED CT
763795006
UMLS CUI
C3553660
Fully Specified Name
Malan overgrowth 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.