Diseases and Disorders > Genetics and Birth Defects

Use these links to jump directly to your topic of interest in Genetics and Birth Defects:

Genetics: General Genetics | Gene Therapy | Genetic Counseling | Genetic Testing | Genetics of Specific Diseases

Birth Defects: General Birth Defects | Cardiovascular Defects | Connective Tissue Disorders | Craniofacial Anomalies | Digestive System Defects | Dwarfism | Eye Abnormalities | Genital Defects | Musculoskeletal Defects | Nervous System Defects | Multiple Congenital Anomalies: #, A - C, D - M, N - R , S - W | Urinary Tract Defects

Multiple Congenital Anomalies (N - R)

(Jump to: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z )

	Nail Patella Syndrome
	FAQ Concerning Nail Patella Syndrome:Nail Patella Syndrome Worldwide
	Nail Patella Syndrome:Carol Ferensak (patient)
	Nail-Patella Syndrome:Genetics Home Reference, NLM
	Nail-Patella Syndrome:GeneReviews

	Nijmegen Breakage Syndrome
	Nijmegen Breakage Syndrome:Madisons Foundation
	Patient Care and Treatment:Nijmegen Breakage Syndrome
	Nijmegen Breakage Syndrome:GeneReviews

	Noonan Syndrome
	Noonan Syndrome:Madisons Foundation
	Noonan Syndrome:Birth Defects Foundation, UK [PDF] [Order printed copy]
	Noonan Syndrome:Swedish Information Center for Rare Diseases
	Noonan Syndrome:Genetics Home Reference, NLM
	Noonan Syndrome:GeneReviews

	Norrie Disease
	Norrie Disease:Madisons Foundation
	Norrie Disease:Genetics Home Reference, NLM
	NDP-Related Retinopathies:GeneReviews

	Opitz G/BBB Syndrome
	Opitz G/BBB Syndrome:NORD
	Opitz G/BBB Syndrome:Genetics Home Reference, NLM
	X-Linked Opitz G/BBB Syndrome:GeneReviews
	See also 22q11.2 Deletion Syndrome

	Oral Facial Digital Syndrome
	Oral-Facial-Digital Syndrome:NORD
	Oral-Facial-Digital Syndrome I and II:Swedish Information Center for Rare Diseases
	Oral-Facial-Digital Syndrome Type I:GeneReviews

	Otopalatodigital Spectrum Disorders
	General Information:OPD Syndrome Family Resource Network
	Frontometaphyseal Dysplasia:Genetics Home Reference, NLM
	Melnick-Needles Syndrome:Genetics Home Reference, NLM
	Otopalatodigital Syndrome Type 1:Genetics Home Reference, NLM
	Otopalatodigital Syndrome Type 2:Genetics Home Reference, NLM
	Otopalatodigital Spectrum Disorders:GeneReviews

	Pallister-Hall Syndrome
	Pallister-Hall Syndrome:Madisons Foundation
	Pallister-Hall Syndrome:Genetics Home Reference, NLM
	Pallister-Hall Syndrome:GeneReviews

	Pendred Syndrome
	Pendred Syndrome:Madisons Foundation
	Pendred Syndrome:Genetics Home Reference, NLM
	Pendred Syndrome/DFNB4:GeneReviews

	Peters Anomaly
	Krause Kivlin Syndrome:Madisons Foundation
	Peters Anomaly / Peters Plus Syndrome:Contact a Family, UK
	Peters Plus Syndrome:Genetics Home Reference, NLM
	Peters Plus Syndrome:GeneReviews

	Pfeiffer Syndrome
	Pfeiffer Syndrome:FACES
	Pfeiffer Syndrome:Craniofacial Center
	Pfeiffer Syndrome:Johns Hopkins Craniofacial Center
	Pfeiffer Syndrome:Genetics Home Reference, NLM
	See also Craniofacial Anomalies, Craniosynostosis

	Pierre Robin Sequence
	Pierre Robin Sequence:FACES
	Pierre Robin Sequence/Complex:Cleft Palate Foundation
	Pierre Robin Network

	Poland Syndrome
	Poland Syndrome:Madisons Foundation
	FAQ:Polands-Syndrome.com
	Learning About Poland Anomaly:NHGRI

	Prader-Willi Syndrome
	Prader-Willi Syndrome (PWS):University of Michigan Health System
	Questions and Answers on Prader-Willi Syndrome:Prader-Willi Syndrome Association
	Prader-Willi Syndrome Brochures:Prader-Willi Syndrome Association
	Prader-Willi Syndrome:Swedish Information Center for Rare Diseases
	Prader-Willi Syndrome:Angelman, Rett, and Prader-Willi Syndrome Consortium
	Prader-Willi Syndrome:Genetics Home Reference, NLM
	Prader-Willi Syndrome:GeneReviews
	Prader-Willi Syndrome:MedlinePlus

	Proteus Syndrome
	Proteus Syndrome:Madisons Foundation
	Common Signs of Proteus Syndrome:Proteus Syndrome Foundation, UK
	See also Vascular Anomalies

	Prune Belly Syndrome
	Prune Belly Syndrome:Madisons Foundation
	Prune Belly Syndrome Medical Information:Prune Belly Syndrome Network

	Roberts Syndrome
	Roberts Syndrome:NORD
	Roberts Syndrome:GeneReviews

	Robinow Syndrome
	Robinow Syndrome:Madisons Foundation
	General Information:Robinow Syndrome Foundation
	Robinow Syndrome:Genetics Home Reference, NLM
	ROR2-Related Robinow Syndrome:GeneReviews

	Rothmund-Thomson Syndrome
	Rothmund-Thomson Syndrome:Madisons Foundation
	Rothmund-Thomson Syndrome:Genetics Home Reference, NLM
	Rothmund-Thomson Syndrome:GeneReviews
	See also Ectodermal Dysplasia

	Rubinstein-Taybi Syndrome
	Rubensein-Taybi Syndrome Pamphlet:Rubenstein-Taybi Syndrome
	Book for Families:Rubenstein-Taybi Syndrome
	Rubinstein-Taybi Syndrome:Swedish Information Center for Rare Diseases
	Rubinstein-Taybi Syndrome:Genetics Home Reference, NLM
	Rubinstein-Taybi Syndrome:GeneReviews

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