- 1968.
Vohwinkel syndrome (also
known as "Keratoderma
hereditaria mutilans", "Keratoma
hereditaria mutilans", "Mutilating
keratoderma of Vohwinkel",: 213 ...
-
Keratoendotheliitis fugax hereditaria is an
autosomal dominantly inherited disease of the cornea,
caused by a
point mutation in
cryopyrin (also known...
-
Dyschromatosis symmetrica hereditaria (also
known as "reticulate
acropigmentation of Dohi", and "symmetrical
dyschromatosis of the extremities") is a...
-
Dyschromatosis universalis hereditaria is a type of
pigmentation disorder of the skin. It is
characterized by dark and
light spots formed like lace in...
- (1956). "Infantile
genetic agranulocytosis;
agranulocytosis infantilis hereditaria". Acta Paediatr. 45 (Suppl 105): 1–78. doi:10.1111/j.1651-2227.1956.tb06875...
-
genetic mutation and
pathogenic pathway, and
keratoendotheliitis fugax hereditaria in
which the
autoinflammatory symptoms affect only the
anterior segment...
-
leucism Hyper-
Dyschromia Dyschromatosis symmetrica hereditaria Dyschromatosis universalis hereditaria See also Skin
color Skin
whitening Tanning Sunless...
-
multisystem inflammatory disease (NOMID), and
keratoendotheliitis fugax hereditaria.
Defects in this gene have also been
linked to
familial Mediterranean...
-
Umwelthilfe e. V., a
German environmental NGO
Dyschromatosis universalis hereditaria, a
hereditary skin
disorder DUH, FAA code for
Toledo Suburban Airport...
- A
captaincy (Spanish: capitanía [kapitaˈni.a], Portuguese:
capitania [kɐpitɐˈni.ɐ], Croatian: kapetanija) is a
historical administrative division of the...
