Isolated ACF (asymmetric crying facies)

disorder

SNOMED 1345054009CUI C5968342

Overview

Isolated ACF (asymmetric crying facies) 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.

Hypoplasia of depressor angula oris muscle

Very frequent (80-99%)HP:0011333

Malformation of the lower lip

Very frequent (80-99%)HP:0000178

Cerebral cortex atrophy

Frequent (30-79%)HP:0002120

Cleft of palate

Frequent (30-79%)HP:0000175

Cryptorchidism

Frequent (30-79%)HP:0000028

Decreased body height

Frequent (30-79%)HP:0004322

Decreased size of cranium

Frequent (30-79%)HP:0000252

Dental agenesis

Frequent (30-79%)HP:0009804

Diaphragmatic hernia

Frequent (30-79%)HP:0000776

Hypertonia

Frequent (30-79%)HP:0001276

Hypoplastic mandible

Frequent (30-79%)HP:0000347

Multiple kidney cysts

Frequent (30-79%)HP:0005562

Protruding ear

Frequent (30-79%)HP:0000411

Renal hypoplasia/aplasia

Frequent (30-79%)HP:0008678

Respiratory insufficiency

Frequent (30-79%)HP:0002093

Stiff joint

Frequent (30-79%)HP:0001387

VUR

Frequent (30-79%)HP:0000076

Abnormal aortic morphology

Occasional (5-29%)HP:0001679

Abnormal spinal segmentation

Occasional (5-29%)HP:0003422

Abnormality of cardiovascular system morphology

Occasional (5-29%)HP:0030680

Abnormality of lung artery

Occasional (5-29%)HP:0004414

Abnormality of the hips

Occasional (5-29%)HP:0003272

Abnormality of the respiratory system

Occasional (5-29%)HP:0002086

Mental and motor retardation

Occasional (5-29%)HP:0001263

Tetrology of fallot

Occasional (5-29%)HP:0001636

VSD

Occasional (5-29%)HP:0001629

Related Conditions

Autosomal dominant hereditary disorder(parent)

Hypoplasia of muscle(parent)

Developmental hereditary disorder(parent)

Hereditary disorder of musculoskeletal system(parent)

Congenital anomaly of face(parent)

Congenital anomaly of skeletal muscle(parent)

Disorder of soft tissue of head(parent)

Quick Facts

SNOMED CT: 1345054009
UMLS CUI: C5968342
Fully Specified Name: Congenital unilateral hypoplasia of depressor anguli oris (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 26

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.