Diprosopus

disorder

SNOMED 62192003CUI C0266731

Overview

Diprosopus 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 RPE

Very frequent (80-99%)HP:0007703

Abnormality of the face

Very frequent (80-99%)HP:0000271

Abnormality of vision

Very frequent (80-99%)HP:0000504

Cleft of palate

Very frequent (80-99%)HP:0000175

Dysplastic ears

Very frequent (80-99%)HP:0000377

Eye disease

Very frequent (80-99%)HP:0000478

Fetal anencephaly

Very frequent (80-99%)HP:0002323

Heart septal defect

Very frequent (80-99%)HP:0001671

Nasal deformity

Very frequent (80-99%)HP:0000366

Non-midline cleft of the upper lip

Frequent (30-79%)HP:0100335

Related Conditions

Cephalodiprosopus(child)

Diprosopus tetrophthalmus(child)

Opodidymus(child)

Janiceps(child)

Double lip(child)

Congenital duplication of nose(child)

Duplication of eyebrow and syndactyly syndrome(child)

Congenital distichiasis(child)

Congenital anomaly of face(parent)

Quick Facts

SNOMED CT: 62192003
UMLS CUI: C0266731
Fully Specified Name: Diprosopus (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 10

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.