Hall Riggs syndrome

disorder

SNOMED 721008000CUI C1856198

Overview

Hall Riggs 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.

Decreased body height

Very frequent (80-99%)HP:0004322

Decreased size of cranium

Very frequent (80-99%)HP:0000252

Global developmental delay, severe

Very frequent (80-99%)HP:0011344

Increased width of bridge of nose

Very frequent (80-99%)HP:0000431

Mental retardation, severe

Very frequent (80-99%)HP:0010864

No speech development

Very frequent (80-99%)HP:0001344

Nostrils anteverted

Very frequent (80-99%)HP:0000463

Palpebronasal fold

Very frequent (80-99%)HP:0000286

Prominent lips

Very frequent (80-99%)HP:0012471

Abnormal metaphysis morphology

Frequent (30-79%)HP:0000944

Anomaly of the epiphyses

Frequent (30-79%)HP:0005930

Brachydactyly

Frequent (30-79%)HP:0001156

Cobb angle greater than ten degrees

Frequent (30-79%)HP:0002650

Delayed skeletal development

Frequent (30-79%)HP:0002750

Downturned corners of mouth

Frequent (30-79%)HP:0002714

Epilepsy

Frequent (30-79%)HP:0001250

Flattened vertebral bodies

Frequent (30-79%)HP:0000926

Hyperplasia of nose

Frequent (30-79%)HP:0000448

Increased distance between eyes

Frequent (30-79%)HP:0000316

Large mouth

Frequent (30-79%)HP:0000154

Nausea and vomiting

Frequent (30-79%)HP:0002017

Poor weight gain

Frequent (30-79%)HP:0001508

Rough hair texture

Frequent (30-79%)HP:0002208

Short limbs

Frequent (30-79%)HP:0009826

Slow rate of hair growth

Frequent (30-79%)HP:0002217

Thick hair

Frequent (30-79%)HP:0100874

Delayed eruption of teeth

Occasional (5-29%)HP:0000684

Dystrophic tooth enamel

Occasional (5-29%)HP:0000682

Stiff joint

Occasional (5-29%)HP:0001387

Carp-shaped mouth

HP:0010806

Related Conditions

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

Recessive hereditary disorder (autosomal)(parent)

Spondylometaphyseal dysplasia(parent)

Congenital anomaly of skeletal bone(parent)

Congenital microcephalus(parent)

Genetic intellectual disability(parent)

Quick Facts

SNOMED CT: 721008000
UMLS CUI: C1856198
Fully Specified Name: Hall Riggs 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.