Absence of fingerprints with congenital milia syndrome

disorder

SNOMED 719595002CUI C4304581

Overview

Absence of fingerprints with congenital milia 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 dermatoglyphics

Very frequent (80-99%)HP:0007477

Milia

Very frequent (80-99%)HP:0001056

Skin bullae

Very frequent (80-99%)HP:0008066

Thin skin

Very frequent (80-99%)HP:0000963

Decreased sweating

Frequent (30-79%)HP:0000966

Pachydermia

Frequent (30-79%)HP:0001072

Proximal interphalangeal finger joint contractures

Frequent (30-79%)HP:0100490

Skin rash

Frequent (30-79%)HP:0000988

Pseudoainhum

Occasional (5-29%)HP:0009775

Related Conditions

Autosomal dominant hereditary disorder(parent)

Abnormal dermatoglyphic pattern(parent)

Milia(parent)

Hereditary disorder of the integument(parent)

Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT: 719595002
UMLS CUI: C4304581
Fully Specified Name: Absence of fingerprints with congenital milia syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 9

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.