dyschromatosis symmetrica hereditaria - Ontology Browser

Ontology Browser

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

pigmentation disease + is-a

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

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

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