A (21) | B (52) | C (22) | D (74) | E (10) | F (11) | H (11) | I (2) | J (1) | K (1) | L (5) | M (11) | N (10) | O (5) | P (8) | R (1) | S (21) | T (13) | V (3) | X (5)
Title Type
Carrier screening programs Feature
Carrier screening thalassemia Symptom
CDKL5 deficiency Rare Condition
Cerebral palsy Disease
Cervical block vertebrae Symptom
Cheek bones (small) Feature
Chromosome 21 Down syndrome Rare Condition
Chromosome Ring 20 Syndrome Rare Condition
Chromosome Ring 20 Syndrome General Medical Guideline
Chronic fatigue, unspecified Disease
Cleidocranial Dysplasia / Dysostosis General Medical Guideline
Cleidocranial Dysplasia in family Symptom
Cleidocranial Dysplasia or Dysostosis Rare Condition
Coffin Lowry Syndrome General Medical Guideline
Coffin Lowry Syndrome Rare Condition
Conductive hearing loss Disease
Congenital hallux valgus Symptom
Congenital hallux valgus Disease
Congenital vertebral anomaly guideline Specific Medical Guideline
Conjugated Hyperbilirubinemia Symptom
Craniosynostosis Disease
Creatine-kinase in plasma or serum Feature