Birth Defects - Syndromes - Malformations - Anomalies
- C
- C Cell Carcinoma
- C Cell Carcius
- CA21H
- Cafe-Au-Lait Spots, Multiple as part of NF
- CAH
- Campomelic Dysplasia
- Cancer
- Capillary - Venous Leptomeningeal Angiomatosis
- Cardiac Malformations
- Cardio Velo Facial
- Cardiomyopathic Multiple Lentigines in context of NF
- Cardiovascular Defects
- Cat Cry
- Cat Eye
- CATCH22
- CENPC 1
- CENPC 2
- Central Type Neurofibromatosis
- Centromeric Protein C1
- Centromeric Protein C1 Pseudogene
- Cerebral Palsy
- CES
- Chandler
- CHARGE
- Chat Cri Du
- Chernobyl Radiation
- Cholestasis With Peripheral Pulmonary Artery Stenosis
- Chornobyl Radiation
- Chromosomal Instability And Immunodeficiency Microcephaly
- Chromosome 1q32
- Chromosome 5 Deletion
- Chromosome 5p-
- Chromosome 8
- Chromosome 8 Deletion
- Chromosome 11p Deletion
- Chromosome 11p-
- Chromosome 22 Deletion
- Chromosome 22 related Syndromes
- Chromosome 22q-
- Circumcision Female Pharaonic
- Cleft Lip and Palate
- Cleft Lip and / or Palate with Mucous Cysts of Lower Lip
- Cloacal Exstrophy
- Cloacal Sequence
- Clubfoot
- CMV
- Cocaine
- Cogan-Reese
- Collins Treacher Franceschetti
- Colorectal Cancer
- Congenital Absence of the Abdominal Muscles
- Congenital Adrenal Hyperplasia
- Congenital Adrenal Hyperplasia
- Congenital Amputation
- Congenital Articular Rigidity
- Congenital Constricting Band
- Congenital Contractures
- Congenital Cytomegalovirus
- Congenital Diaphragmatic Hernia
- Congenital Heart Disease
- Congenital Herpes Simplex
- Congenital Hydantoin
- Congenital Infections
- Congenital Mixovirus
- Congenital Mumps
- Congenital Nephrotic Syndrome
- Congenital Syphilis
- Congenital Toxoplasmosis
- Conjoined Twins
- Conotruncal Face
- Contractural Arachnodactyly
- Convulsion
- Cords Spinal (Tethered)
- Corneal Irido Endothelial
- Corney Complex
- Coup De Sabre
- CP
- Craniofacial
- Craniofacial Dystosis
- Craniostenosis
- Craniostenosis, Crouzon Type
- Craniosynostoses
- Craniosynostosis
- Crest
- Crst
- Cretinism
- Cri Du Chat
- Crouzon
- Crouzon Pseudo
- Crouzon Craniofacial Dystosis
- Crouzon Type Craniostenosis
- Cry Cat
- Cryptorchidism
- Cryptorchidism
- CYP21 Deficiency
- Cytochrome P450, Subfamily
- Cytochrome P450, Subfamily XIB, Polypeptide
- Cytochrome P450, Subfamily XXI
- Cytochrome P450, Subfamily XXIA
- Cytomegalic Inclusion Disease
- Cytomegalovirus
