Title | Type |
---|---|
Autosomal recessive disease | Feature |
Autosomal dominant mental retardation-50 | Rare Condition |
Autosomal dominant mental retardation-50 | General Medical Guideline |
Autosomal dominant mental retardation-18 | Rare Condition |
Autosomal dominant inheritance in TCS | Symptom |
Autosomal dominant inheritance | Feature |
Autosomaal dominante mentale retardatie-50 | Symptom |
Autism | Disease |
Aural Atresia | Disease |
Antimongoloid slanting palpebral fissures | Feature |
Antimongoloid slanting palpebral fissures | Symptom |
Anterior fontanelle persists | Symptom |
Anterior fontanelle closure | Feature |
Anemia in thalassemia | Symptom |
Anemia in Sickle Cell Disease | Symptom |
Alport Syndrome | Rare Condition |
Alport Syndrome | General Medical Guideline |
Alagille Syndrome | Rare Condition |
Alagille Syndrome | General Medical Guideline |
Acute chest syndrome | Disease |
Abnormal hands | Feature |