Overview
Genitopalatocardiac 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.
Abnormality of cardiovascular system morphology
Very frequent (80-99%)HP:0030680
Decreased projection of mandible
Very frequent (80-99%)HP:0000347
Heart septal defect
Very frequent (80-99%)HP:0001671
Low-set ears
Very frequent (80-99%)HP:0000369
Male pseudohermaphroditism
Very frequent (80-99%)HP:0000037
Non-midline cleft of the upper lip
Very frequent (80-99%)HP:0100335
Small for gestational age infant
Very frequent (80-99%)HP:0001511
Cryptorchidism
Frequent (30-79%)HP:0000028
Down-slanting palpebral fissure
Frequent (30-79%)HP:0000494
Gonadal dysgenesis, male
Frequent (30-79%)HP:0008668
Hypospadias
Frequent (30-79%)HP:0000047
Abnormal mesentery morphology
Occasional (5-29%)HP:0100016
Abnormality of the gallbladder
Occasional (5-29%)HP:0005264
Brachydactyly
Occasional (5-29%)HP:0001156
Broad flat nasal bridge
Occasional (5-29%)HP:0000431
Cobb angle greater than ten degrees
Occasional (5-29%)HP:0002650
Decreased size of cranium
Occasional (5-29%)HP:0000252
Diaphragmatic hernia
Occasional (5-29%)HP:0000776
Downturned corners of mouth
Occasional (5-29%)HP:0002714
Hunched back
Occasional (5-29%)HP:0002808
Increased distance between eyes
Occasional (5-29%)HP:0000316
Multicystic kidney dysplasia
Occasional (5-29%)HP:0000003
Nonsyndromal hydrocephalus
Occasional (5-29%)HP:0000238
Postaxial hand polydactyly
Occasional (5-29%)HP:0001162
Cleft of palate
HP:0000175
Cleft of upper lip
HP:0000204
Double-outlet right ventricle
HP:0001719
Renal cyst
HP:0000107
Right aortic arch
HP:0012020
Transposition of great vessels
HP:0001669
Related Conditions
Congenital heart disease(parent)
Cleft palate(parent)
Recessive hereditary disorder (autosomal)(parent)
Cardiovascular system hereditary disorder(parent)
Reproductive system hereditary disorder(parent)
Multiple system malformation syndrome(parent)
Pure gonadal dysgenesis 46,XY(parent)
Developmental hereditary disorder(parent)
Quick Facts
- SNOMED CT
- 773749003
- UMLS CUI
- C1856466
- Fully Specified Name
- Genitopalatocardiac syndrome (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.