Details of Disease | DrugMAP

General Information of Disease (ID: DIS2MULR)

Disease Name	Hyperpigmentation with or without hypopigmentation, familial progressive
Synonyms	FPHH; melanosis universalis hereditaria; hyperpigmentation, familial progressive, 2; hyperpigmentation, familial progressive, 2, formerly; hyperpigmentation with or without hypopigmentation; melanosis, universal; macules, hereditary congenital hypopigmented and hyperpigmented; hyperpigmentation with or without hypopigmentation, familial progressive
Disease Hierarchy	DISVYG2G: Familial progressive hyperpigmentation DISSCALK: Hereditary skin disorder DIS2MULR: Hyperpigmentation with or without hypopigmentation, familial progressive
Disease Identifiers	MONDO ID MONDO_0007771 UMLS CUI C1840392 OMIM ID 145250 MedGen ID 333550 SNOMED CT ID 715630006

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTT Molecule(s)

Gene Name	DTT ID	Evidence Level	Mode of Inheritance	REF
KITLG	TTDJ51N	Strong	Genetic Variation	[1]
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References

1	Familial progressive hyper- and hypopigmentation: a report on a Chinese family and evidence for genetic heterogeneity.An Bras Dermatol. 2017 May-Jun;92(3):329-333. doi: 10.1590/abd1806-4841.20175567.