Cloverleaf skull with multiple congenital anomalies syndrome

disorder

SNOMED 717771007CUI C1846671

Overview

Cloverleaf skull with multiple congenital anomalies 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.

Abnormal clavicles

Very frequent (80-99%)HP:0000889

Abnormal metaphysis morphology

Very frequent (80-99%)HP:0000944

Anomaly of the epiphyses

Very frequent (80-99%)HP:0005930

Bowed long bones

Very frequent (80-99%)HP:0006487

Cloverleaf skull shape

Very frequent (80-99%)HP:0002676

Decreased height of philtrum

Very frequent (80-99%)HP:0000322

Downturned corners of mouth

Very frequent (80-99%)HP:0002714

Flattened vertebral bodies

Very frequent (80-99%)HP:0000926

Frontal protuberance

Very frequent (80-99%)HP:0002007

Hypoplastic mandible condyle

Very frequent (80-99%)HP:0000347

Increased basal angle of skull base

Very frequent (80-99%)HP:0002691

Increased distance between eyes

Very frequent (80-99%)HP:0000316

Increased width of bridge of nose

Very frequent (80-99%)HP:0000431

Low chest circumference

Very frequent (80-99%)HP:0000774

Low-set ears

Very frequent (80-99%)HP:0000369

Poorly ossified skull

Very frequent (80-99%)HP:0004331

Rhizomelic limb shortening

Very frequent (80-99%)HP:0008905

Rib anomalies

Very frequent (80-99%)HP:0000772

Short neck

Very frequent (80-99%)HP:0000470

Abnormally small eyeball

Frequent (30-79%)HP:0000568

Absence of corpus callosum

Frequent (30-79%)HP:0001274

Ambiguous external genitalia

Frequent (30-79%)HP:0000062

Attachment of thumb close to wrist

Frequent (30-79%)HP:0009623

Cataract

Frequent (30-79%)HP:0000518

Omphalocoele

Frequent (30-79%)HP:0001539

VSD

Frequent (30-79%)HP:0001629

Wide bregma sutures

Frequent (30-79%)HP:0000239

Related Conditions

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

Longitudinal deficiency of limb(parent)

Recessive hereditary disorder (autosomal)(parent)

Clover leaf skull deformity(parent)

Hereditary disorder of musculoskeletal system(parent)

Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT: 717771007
UMLS CUI: C1846671
Fully Specified Name: Cloverleaf skull with multiple congenital anomalies syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 27

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.