Tatton Brown Rahman overgrowth syndrome

disorder

SNOMED 768843007CUI C4014545

Overview

Tatton Brown Rahman 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.

Arnold Chiari type I malformation

Always present (100%)HP:0007099

Cupid-bow shaped upper lip

Always present (100%)HP:0002263

Decreased volume of lip vermillion

Always present (100%)HP:0000233

Febrile seizure (within the age range of 3 months to 6 years)

Always present (100%)HP:0002373

Foetal distress

Always present (100%)HP:0025116

General overgrowth

Always present (100%)HP:0001548

Lack of eyebrow curvature

Always present (100%)HP:0011228

Mental and motor retardation

Always present (100%)HP:0001263

Mental-retardation

Always present (100%)HP:0001249

Muscular hypotonia

Always present (100%)HP:0001252

Nostrils anteverted

Always present (100%)HP:0000463

Palpebronasal fold

Always present (100%)HP:0000286

Protruding upper lip

Always present (100%)HP:0010803

Talipes valgus

Always present (100%)HP:0004684

VSD

Always present (100%)HP:0001629

Accelerated linear growth

Very frequent (80-99%)HP:0000098

Increased size of skull

Very frequent (80-99%)HP:0000256

Proportionate tall stature

Very frequent (80-99%)HP:0011407

Behavioral changes

Frequent (30-79%)HP:0000708

Cobb angle greater than ten degrees

Frequent (30-79%)HP:0002650

Hypotonia, early

Frequent (30-79%)HP:0008947

Kyphoscoliosis

Frequent (30-79%)HP:0002751

Moderate mental retardation

Frequent (30-79%)HP:0002342

Obesity

Frequent (30-79%)HP:0001513

Anxiety disease

Occasional (5-29%)HP:0000739

Atria septal defect

Occasional (5-29%)HP:0001631

Chiari malformation

Occasional (5-29%)HP:0002308

Cryptorchidism

Occasional (5-29%)HP:0000028

Diastema between maxillary central incisors

Occasional (5-29%)HP:0001566

Dilated cerebral ventricle

Occasional (5-29%)HP:0002119

Related Conditions

Multiple malformation syndrome with early overgrowth(parent)

Disorder of stature(parent)

Multiple malformation syndrome with facial defects as major feature(parent)

Genetic intellectual disability(parent)

Quick Facts

SNOMED CT: 768843007
UMLS CUI: C4014545
Fully Specified Name: Tall stature, intellectual disability, facial dysmorphism 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.