FTP Download
Chinchilla Research Resource Database
   
Keyword
  

Ontology Browser

Term:
Waardenburg Syndrome Type 4 (DOID:9005027)
Annotations: Rat: (6) Mouse: (4) Human: (5) Chinchilla: (4) Bonobo: (4) Dog: (4) Squirrel: (4)
Parent Terms Term With Siblings Child Terms
ABCD syndrome  
acanthosis nigricans +   
ADULT syndrome  
Al Gazali Hirschsprung Syndrome 
Anonychia with Flexural Pigmentation 
Argyria 
BADS syndrome 
Basaran Yilmaz Syndrome  
Bloch-Sulzberger syndrome +   
Bresheck/Bresek Syndrome 
Bullous Dystrophy, Hereditary Macular Type 
Cafe-au-Lait Spots +   
Cartilage Hair Hypoplasia Like Syndrome 
cartilage-hair hypoplasia  
conjunctival pigmentation 
dyschromatosis symmetrica hereditaria  
dyschromatosis universalis hereditaria +   
Elejalde Disease 
FLOTCH Syndrome 
Goldberg-Shprintzen syndrome  
Graying of Hair, Precocious 
Griscelli syndrome +   
Grouped Pigmentation of the Macula 
Heterochromia Iridis  
Hirschsprung Disease 1  
Hirschsprung Disease Ganglioneuroblastoma  
Hirschsprung Disease Polydactyly Heart Disease 
Hirschsprung Disease Type 3 
Hirschsprung Disease Type d Brachydactyly 
Hirschsprung Disease with Heart Defects, Laryngeal Anomalies, and Preaxial Polydactyly 
Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness 
Hirschsprung Disease with Ulnar Polydactyly, Polysyndactyly of Big Toes, and Ventricular Septal Defect 
Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction  
Hyperpigmentation +   
Hypopigmentation +   
hypopigmentation of eyelid 
Laurence Prosser Rocker Syndrome 
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis 
Macules Hereditary Congenital Hypopigmented and Hyperpigmented 
microphthalmia with limb anomalies  
Mowat-Wilson syndrome  
neonatal jaundice +   
Oculocerebral Hypopigmentation Syndrome Type Preus 
PCWH syndrome  
Pigmented Purpuric Eruption 
Red Skin Pigment Anomaly of New Guinea 
Reticulate Pigmentary Disorder, with Systemic Manifestations  
Russell-Silver Syndrome, X-Linked 
Santos Mateus Leal Syndrome 
Skin/Hair/Eye Pigmentation, Variation In, 1  
Skin/Hair/Eye Pigmentation, Variation In, 10  
Skin/Hair/Eye Pigmentation, Variation In, 11  
Skin/Hair/Eye Pigmentation, Variation In, 4  
Skin/Hair/Eye Pigmentation, Variation In, 5  
Skin/Hair/Eye Pigmentation, Variation In, 6  
Skin/Hair/Eye Pigmentation, Variation In, 7  
Skin/Hair/Eye Pigmentation, Variation In, 8  
Skin/Hair/Eye Pigmentation, Variation In, 9  
stromal corneal pigmentation 
Symmetric Acroleukopathy 
Tang Hsi Ryu Syndrome 
Terminal Osseous Dysplasia and Pigmentary Defects  
Thumb Deformity, Alopecia, Pigmentation Anomaly 
Total Intestinal Aganglionosis  
urticaria pigmentosa  
Van der Hoeve Halbertsma Waardenburg Gualdi Syndrome 
Waardenburg syndrome type 1  
Waardenburg syndrome type 2A  
Waardenburg syndrome type 2B 
Waardenburg syndrome type 2C 
Waardenburg syndrome type 2D  
Waardenburg syndrome type 2E  
Waardenburg syndrome type 3  
Waardenburg Syndrome Type 4 +   
Waardenburg syndrome type 4A  
Waardenburg syndrome type 4B  
Waardenburg syndrome type 4C  
White Forelock with Malformations 
Whyte Murphy Syndrome 
xeroderma pigmentosum +   
yellow nail syndrome +  

Synonyms
Exact Synonyms: Hirschsprung disease with pigmentary anomaly ;   Shah-Waardenburg syndrome ;   WS4 ;   Waardenburg-Hirschsprung disease
Primary IDs: MESH:C536467
Alternate IDs: RDO:0002060

paths to the root