|  Help  |  About  |  Contact Us

DO Term : familial progressive hyperpigmentation with or without hypopigmentation [DOID:0111373] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A skin disease characterized by progressive, diffuse hyperpigmentation of variable intensity sometimes associated with cafe-au-lait macules and larger hypopigmented ash-leaf macules that has_material_basis_in heterozygous mutation in the KITLG gene on chromosome 12q21.32.
  • synonyms:
  • melanosis universalis hereditaria,
  • OMIM:145250,
  • MUH,
  • FPHH,
  • 145250
Quick Links:
 
Quick Links:
 

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents