Chimera 46, XX; 46, XY

disorder

SNOMED 205718006CUI C0432480

Overview

Chimera 46, XX; 46, XY 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 cellular immune system morphology

Very frequent (80-99%)HP:0010987

Abnormal scrotum morphology

Very frequent (80-99%)HP:0000045

Abnormality of multiple cell lineages in the bone marrow

Very frequent (80-99%)HP:0012145

Abnormality of the ovary

Very frequent (80-99%)HP:0000137

Ambiguous external genitalia

Very frequent (80-99%)HP:0000062

Anomaly of the testes

Very frequent (80-99%)HP:0000035

Blood group antigen abnormality

Very frequent (80-99%)HP:0010970

Cryptorchidism

Very frequent (80-99%)HP:0000028

Hypopigmented skin patches

Very frequent (80-99%)HP:0001053

Ovotestis

Very frequent (80-99%)HP:0012861

Perineal hypospadias

Very frequent (80-99%)HP:0000051

Prominent clitoris

Very frequent (80-99%)HP:0008665

Scrotal cleft

Very frequent (80-99%)HP:0000048

Short penis

Very frequent (80-99%)HP:0000054

True hermaphroditism

Very frequent (80-99%)HP:0010459

Xy female gonadal dysgenesis

Very frequent (80-99%)HP:0008723

Single flexion crease

Frequent (30-79%)HP:0000954

Related Conditions

Chimera(parent)

Quick Facts

SNOMED CT: 205718006
UMLS CUI: C0432480
Fully Specified Name: Chimera 46, XX; 46, XY (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 17

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.