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Pigmentation disorder

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Pigmentation disorder
Classification and external resources
ICD-10 L80-L81
ICD-9 709.01
MeSH D010859

Pigmentation disorders are disturbances of human skin color, either loss or reduction, which may be related to loss of melanocytes or the inability of melanocytes to produce melanin or transport melanosomes correctly.[1]

[edit] References

  1. ^ James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN 0-7216-2921-0.
v · d · e
Pigmentation disorders/Dyschromia (L80–L81, 709.0)
Hypo-/
leucism
Loss of melanocytes
Leukoderma w/o
hypomelanosis
Ungrouped
Hyper-
Reticulated
Diffuse/
circumscribed
Linear
Other/ungrouped
Other
pigments
Dyschromatoses

M: INT, SF, LCT

noco(i/b/d/q/u/r/p/m/k/v/f)/cong/tumr(n/e/d), sysi/epon

proc, drug (D2/3/4/5/8/11)
v · d · e
Congenital malformations and deformations of integument / skin disease (Q80–Q82, 757.0–757.3)
Genodermatosis
Ungrouped
EB
and related
Other
Other
Developmental
anomalies
Midline
Other/ungrouped

Aplasia cutis congenita · Amniotic band syndrome · Branchial cyst · Cavernous venous malformation

Accessory nail of the fifth toe · Bronchogenic cyst · Congenital cartilaginous rest of the neck · Congenital hypertrophy of the lateral fold of the hallux · Congenital lip pit · Congenital malformations of the dermatoglyphs · Congenital preauricular fistula · Congenital smooth muscle hamartoma · Cystic lymphatic malformation · Median raphe cyst · Melanotic neuroectodermal tumor of infancy · Mongolian spot · Nasolacrimal duct cyst · Omphalomesenteric duct cyst · Poland anomaly · Rapidly involuting congenital hemangioma · Rosenthal–Kloepfer syndrome · Skin dimple · Superficial lymphatic malformation · Thyroglossal duct cyst · Verrucous vascular malformation · Birthmark

M: INT, SF, LCT

noco(i/b/d/q/u/r/p/m/k/v/f)/cong/tumr(n/e/d), sysi/epon

proc, drug (D2/3/4/5/8/11)
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