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Ontology Browser

Term:
dyschromatosis symmetrica hereditaria (DOID:0060257)
Annotations: Rat: (2) Mouse: (2) Human: (2) Chinchilla: (2) Bonobo: (2) Dog: (2) Squirrel: (2) Pig: (2)
Parent Terms Term With Siblings Child Terms
acanthosis nigricans +   
ADULT syndrome  
Anonychia with Flexural Pigmentation 
Argyria 
BADS syndrome 
Basaran Yilmaz Syndrome  
Bloch-Sulzberger syndrome +   
Bullous Dystrophy, Hereditary Macular Type 
Cafe-au-Lait Spots +   
Cancer, Alopecia, Pigment Dyscrasia, Onychodystrophy, and Keratoderma  
conjunctival pigmentation 
dyschromatosis symmetrica hereditaria  
A pigmentation disease characterized by progressively pigmented and depigmented macules, often mixed in a reticulate pattern, concentrated on the dorsal extremities. (DO)
dyschromatosis universalis hereditaria +   
Elejalde Disease 
FLOTCH Syndrome 
Griscelli syndrome +   
Grouped Pigmentation of the Macula 
Heterochromia Iridis  
Hyperpigmentation +   
Hypopigmentation +   
hypopigmentation of eyelid 
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis 
Macules Hereditary Congenital Hypopigmented and Hyperpigmented 
neonatal jaundice +   
Oculocerebral Hypopigmentation Syndrome Type Preus 
Pigmented Purpuric Eruption 
Precocious Graying of Hair 
Red Skin Pigment Anomaly of New Guinea 
Reticulate Pigmentary Disorder, with Systemic Manifestations  
Russell-Silver Syndrome, X-Linked 
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 
urticaria pigmentosa  
Waardenburg Syndrome Type 4 +   
White Forelock with Malformations 
Whyte Murphy Syndrome 
xeroderma pigmentosum +   
yellow nail syndrome +  

Synonyms
Exact Synonyms: DSH ;   DSH1 ;   Dyschromatosis Symmetrica Hereditaria 1 ;   Familial reticulate acropigmentation of Dohi ;   RAD ;   Reticulate acropigmentation of Dohi ;   symmetric dyschromatosis of the extremities ;   symmetrical dyschromatosis of extremities
Primary IDs: MESH:C535729
Alternate IDs: OMIM:127400 ;   RDO:0001011
Xrefs: NCI:C118435 ;   ORDO:41
Definition Sources: http://en.wikipedia.org/wiki/Dyschromatosis_symmetrica_hereditaria, http://www.alibris.com/Andrews-Diseases-of-the-Skin-Clinical-Dermatology-Expert-Consult-Online-and-Print-William-D-James-Col/book/28312193?qsort=c&matches=15, https://www.ncbi.nlm.nih.gov/pubmed/22974014

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.