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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
Eclabium of upper lip
Always present (100%)HP:0010803
Febrile seizure (within the age range of 3 months to 6 years)
Always present (100%)HP:0002373
Foetal distress
Always present (100%)HP:0025116
Generalised overgrowth
Always present (100%)HP:0001548
Lack of eyebrow curvature
Always present (100%)HP:0011228
Nonprogressive mental retardation
Always present (100%)HP:0001249
Nostrils anteverted
Always present (100%)HP:0000463
Palpebronasal fold
Always present (100%)HP:0000286
Peripheral hypotonia
Always present (100%)HP:0001252
Psychomotor development deficiency
Always present (100%)HP:0001263
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 symptoms
Frequent (30-79%)HP:0000708
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
Scoliosis
Frequent (30-79%)HP:0002650
Atria septal defect
Occasional (5-29%)HP:0001631
Chiari malformation
Occasional (5-29%)HP:0002308
Coarse face
Occasional (5-29%)HP:0000280
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.