genodermatosis

It is a type of genodermatosis.

Kindler syndrome is an autosomal recessive genodermatosis.

It could be classified as a skin condition, or more precisely as a genodermatosis (a genetically determined skin disorder).

Restrictive dermopathy (RD), also called tight skin contracture syndrome, is a rare, lethal autosomal recessive perinatal genodermatosis.

Dyschromatosis universalis hereditaria is a rare genodermatosis characterized by reticulate hyper- and hypo- pigmentated macules in a generalized distribution.

Bazex-Dupré-Christol syndrome, another rare genodermatosis associated with development of BCC, has more thorough documentation in the literature than Rombo syndrome.

A rare genodermatosis, its key features include "rosacea-like facial eruption[,] reticulated hyperpigmentation of major flexures, comedones on the back and neck, and pitted facial scars."

Requena L, Fariña MC, Robledo M, et al.: Multiple hereditary infundibulocystic basal cell carcinomas: a genodermatosis different from nevoid basal cell carcinoma syndrome.

BIDS syndrome, also called nonphotosensitive trichothiodystrophy 1 (TTND1), Amish brittle hair brain syndrome and hair-brain syndrome, is an autosomal recessive genodermatosis similar to IBIDS syndrome but without the ichthyosiform changes.