← Back to Conditions

Ackerman syndrome

disorder
SNOMED 722280000CUI C1860167

Overview

Ackerman 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.

Glaucoma
HP:0000501
Large elongated pulp chamber
HP:0000679
Wide philtrum
HP:0000289

Related Conditions

Ectodermal dysplasia(parent)
Multiple system malformation syndrome(parent)
Recessive hereditary disorder (autosomal)(parent)
Hereditary disorder of the integument(parent)
Congenital anomaly of tooth(parent)
Developmental hereditary disorder(parent)
Hereditary disorder of tooth(parent)

Quick Facts

SNOMED CT
722280000
UMLS CUI
C1860167
Fully Specified Name
Ackerman syndrome (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
3
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.