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SLC29A3
- H Syndrome
- H Syndrome
- Histiocytosis-Lymphadenopathy Plus Syndrome
CFH
- Complement Factor H Deficiency
- Immunodeficiency With Factor H Anomaly
- Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 1
ATRX
- Hemoglobin H Disease
- Alpha-Thalassemia/mental Retardation Syndrome, X-Linked
CACNA1A
- Spinocerebellar Ataxia Type 6
- Paroxysmal Kinesigenic Choreoathetosis
HBA1
- Hemoglobin H Disease
- Hemoglobin H Disease
HBA2
- Hemoglobin H Disease
- Hemoglobin H Disease
IL1B
- Helicobacter Pylori (H. Pylori) Infection
- Peptic Ulcer
- Spinocerebellar Ataxia Type 6
- Gastritis
- Peptic Ulcer Disease
LAMB3
- Junctional Epidermolysis Bullosa, Generalized Severe
GAST
- Helicobacter Pylori (H. Pylori) Infection
- Peptic Ulcer
- Gastritis
- Malt Lymphoma
- Peptic Ulcer Disease
TBX4
- Ischiopatellar Dysplasia
LAMC2
- Junctional Epidermolysis Bullosa, Generalized Severe
BCL10
- Gastritis
- Malt Lymphoma
SLC34A2
- Pulmonary Alveolar Microlithiasis
TFG
- Hereditary Motor And Sensory Neuropathy With Proximal Dominance
CFHR1
- Complement Factor H Deficiency
- Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 1
CD46
- Immunodeficiency With Factor H Anomaly
- Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 1
- Gastritis
DGKE
- Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 1
TNF
- Helicobacter Pylori (H. Pylori) Infection
- H Syndrome
- H Syndrome
- Peptic Ulcer
- Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 1
- Spinocerebellar Ataxia Type 6
- Gastritis
- Malt Lymphoma
- Peptic Ulcer Disease
- Histiocytosis-Lymphadenopathy Plus Syndrome
LAMA3
- Junctional Epidermolysis Bullosa, Generalized Severe
C3
- Complement Factor H Deficiency
- Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 1