Cutis marmorata telangiectatica congenita

disorder

SNOMED 254778000CUI C0345419

Overview

Cutis marmorata telangiectatica congenita 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.

Abnormality of the arm

Very frequent (80-99%)HP:0002817

Abnormality of the lower limb

Very frequent (80-99%)HP:0002814

Arteriovenous malformation

Very frequent (80-99%)HP:0100026

Bleeding below the skin

Very frequent (80-99%)HP:0001933

Cutis marmorata

Very frequent (80-99%)HP:0000965

Dermatopathy

Very frequent (80-99%)HP:0000951

Seizures

Very frequent (80-99%)HP:0001250

Short lower limbs

Very frequent (80-99%)HP:0006385

Skin erosion

Very frequent (80-99%)HP:0200041

Aplasia/Hypoplasia of the skin

Frequent (30-79%)HP:0008065

Leukocoria

Frequent (30-79%)HP:0000555

Teleangiectasia of the skin

Frequent (30-79%)HP:0100585

Arterial stenosis

Occasional (5-29%)HP:0100545

Capillary hemangioma

Occasional (5-29%)HP:0005306

Cleft lip, cleft palate

Occasional (5-29%)HP:0000202

Cobb angle greater than ten degrees

Occasional (5-29%)HP:0002650

Cognitive deficits

Occasional (5-29%)HP:0100543

Congenital dermal melanocytosis

Occasional (5-29%)HP:0100814

Decreased bone mineral density Z score

Occasional (5-29%)HP:0004349

Decreased projection of lower jaw

Occasional (5-29%)HP:0000347

Displacement of the external urethral orifice

Occasional (5-29%)HP:0100627

Hypothyroidism

Occasional (5-29%)HP:0000821

Multicystic kidney dysplasia

Occasional (5-29%)HP:0000003

Multiple birthmarks

Occasional (5-29%)HP:0007565

Partial syndactyly

Occasional (5-29%)HP:0006101

PDA

Occasional (5-29%)HP:0001643

Peritoneal effusion

Occasional (5-29%)HP:0001541

Red or purple spots on the skin

Occasional (5-29%)HP:0000979

Small for gestational age infant

Occasional (5-29%)HP:0001511

Syndactyly of feet

Occasional (5-29%)HP:0001770

Related Conditions

FILS syndrome(child)

Livedo reticularis(parent)

Congenital vascular disorder(parent)

Fetal and/or neonatal disorder of integument(parent)

Quick Facts

SNOMED CT: 254778000
UMLS CUI: C0345419
Fully Specified Name: Congenital livedo reticularis (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.