Pages that link to "22q11.2 deletion syndrome"
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The following pages link to 22q11.2 deletion syndrome:
Displayed 50 items.
- Cardiofacial Syndrome (redirect page) (← links)
- The genetic basis of heart disease (← links)
- Genetic Disorders (← links)
- Di George syndrome (redirect page) (← links)
- DiGeorges Syndrome (redirect page) (← links)
- Strong Syndrome (redirect page) (← links)
- Chromosome 22 (← links)
- ICD-10 Chapter D (← links)
- List of diseases (0-9) (← links)
- List of genetic disorders (← links)
- Severe combined immunodeficiency (← links)
- Chromosome 22 (human) (← links)
- 22q13 deletion syndrome (← links)
- Myeloperoxidase deficiency (← links)
- WHIM syndrome (← links)
- ZAP70 deficiency (← links)
- TBX1 (← links)
- CATCH 22 syndrome (redirect page) (← links)
- List of diseases starting with a non-letter (← links)
- Asymmetric crying facies (← links)
- Hearing loss with craniofacial syndromes (← links)
- X-linked severe combined immunodeficiency (← links)
- Testpage3 (← links)
- Chromosome 22, microdeletion 22 q11 (redirect page) (← links)
- Velocardiofacial syndrome (redirect page) (← links)
- The genetic basis of heart disease (← links)
- Genetic Disorders (← links)
- List of diseases (V) (← links)
- List of genetic disorders (← links)
- Growth failure (← links)
- Hearing loss with craniofacial syndromes (← links)
- Testpage3 (← links)
- Cerebellar hypoplasia (← links)
- Pierre Robin syndrome (← links)
- Microstomia (← links)
- Macrocephaly (← links)
- Combined immunodeficiency (← links)
- Glossary of medical terms related to communications disorders (← links)
- GP1BB (← links)
- Interrupted aortic arch (patient information) (← links)
- Fabry's disease differential diagnosis (← links)
- Hypothyroidism causes (← links)
- Anxiety causes (← links)
- Arnold-Chiari malformation overview (← links)
- Arnold-Chiari malformation pathophysiology (← links)
- Arnold-Chiari malformation history and symptoms (← links)
- Cyanosis causes (← links)
- Microcephaly causes (← links)
- Hypoparathyroidism pathophysiology (← links)
- Hypoparathyroidism causes (← links)
- Giant platelet disorder (← links)
- Sandbox:Mental retardation causes (← links)
- DGCR2 (← links)
- Shprintzen syndrome (redirect page) (← links)
- The genetic basis of heart disease (← links)
- Genetic Disorders (← links)
- List of diseases (S) (← links)
- List of genetic disorders (← links)
- Oliver's sign (← links)
- Testpage3 (← links)
- List of health topics: Sd-Sh (← links)
- List of health topics: Su-Sy (← links)
- Cyanosis causes (← links)
- Hypoparathyroidism pathophysiology (← links)
- Hypoparathyroidism causes (← links)
- Hyper IgM syndrome (← links)
- ICF syndrome (← links)
- Autosomal dominant opitz G/BBB syndrome (redirect page) (← links)
- Caylor cardiofacial syndrome (redirect page) (← links)
- Conotruncal anomaly face syndrome (redirect page) (← links)
- 22q (redirect page) (← links)
- List of ICD-9 codes 240-279: Endocrine, nutritional and metabolic diseases, and immunity disorders (← links)
- ICD-10 Chapter II: Neoplasms; Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism (← links)
- The WikiDoc Living Textbook of Genetics (← links)
- The WikiDoc Living Textbook of Rheumatology and Autoimmune Disease (← links)
- Monosomy (← links)
- Chromosome 22 deletion syndrome (redirect page) (← links)
- Combined immunodeficiency (← links)
- DiGeorge Syndrome (redirect page) (← links)
- Cri du chat syndrome (← links)
- 22q11 deletion (redirect page) (← links)
- Di George's syndrome (redirect page) (← links)
- DiGeorge syndrome (redirect page) (← links)
- Pulmonary valve stenosis (← links)
- The genetic basis of heart disease (← links)
- Genetic Disorders (← links)
- List of diseases (D) (← links)
- List of genetic disorders (← links)
- Branchial pouch (← links)
- Cytogenetics (← links)
- Growth failure (← links)
- Hypoplasia (← links)
- Testpage3 (← links)
- Delusion (← links)
- Scientific theories regarding acupuncture (← links)
- List of ICD-9 codes 240-279: Endocrine, nutritional and metabolic diseases, and immunity disorders (← links)
- Hypertelorism (← links)
- Combined immunodeficiency (← links)
- List of eponymous diseases (← links)
- SMTN (← links)
- ARVCF (← links)
- HIRA (← links)
- Pharyngeal pouch (embryology) (← links)
- Proline oxidase (← links)
- Interrupted aortic arch (patient information) (← links)
- Persistent truncus arteriosus clinical manifestations (← links)
- Congenital heart disease pathophysiology (← links)
- Tetralogy of fallot(patient information) (← links)
- Tetralogy of fallot causes (← links)
- Interrupted aortic arch overview (← links)
- Bronchiectasis causes (← links)
- Neuroblastoma pathophysiology (← links)
- Neuroblastoma history and symptoms (← links)
- HIV AIDS differential diagnosis (← links)
- 22q11.2 deletion syndrome medical therapy (← links)
- Mental retardation other diagnostic studies (← links)
- Cyanosis causes (← links)
- Acrocyanosis causes (← links)
- Hypoparathyroidism pathophysiology (← links)
- Hypoparathyroidism causes (← links)
- Primary immunodeficiency classification (← links)
- Facial nerve paralysis causes (← links)
- WBR0112 (← links)
- WBR0139 (← links)
- WBR0479 (← links)
- Sandbox:patho2 (← links)
- Candidiasis (← links)
- DGCR8 (← links)
- DGCR2 (← links)
- MRPL40 (← links)
- LZTR1 (← links)
- DGCR5 (← links)
- TANGO2 (← links)
- DGCR6 (← links)
- Aortopulmonary Window (← links)
- DiGeorge's Syndrome (redirect page) (← links)
- Di George Syndrome (redirect page) (← links)
- Hyper-IgM syndrome type 1 (← links)
- Hyper-IgM syndrome type 2 (← links)
- Hyper-IgM syndrome type 3 (← links)
- Hyper-IgM syndrome type 4 (← links)