Hereditary photodermatosis

MONDO:0015951

Hereditary photodermatoses are a spectrum of rare photosensitive disorders that are often caused by genetic deficiency or malfunction of various components of the DNA repair pathway. This results clinically in extreme photosensitivity, with many syndromes exhibiting an increased risk of cutaneous malignancies.

Also known as: photogenodermatosis, photogénodermatose, genetic photosensitivity, genetic skin photosensitivity

31 clinical trials for this condition and its sub-types, 0 tagged with Hereditary photodermatosis itself.

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Where it sits in the disease tree

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Part of

↑ Hereditary skin disorder (885)

Sub-types of Hereditary photodermatosis

Inherited porphyria 0 trials · 24 incl. sub-types
9 sub-types
- Erythropoietic protoporphyria 15 trials Sub-types →
- CPOX-related hereditary coproporphyria 0 trials · 5 incl. sub-types Sub-types →
- HMBS-related hepatic porphyria 0 trials · 5 incl. sub-types Sub-types →
- PPOX-related hepatic porphyria 0 trials · 2 incl. sub-types Sub-types →
- Cutaneous porphyria 2 trials
- UROD-related inherited porphyria 0 trials · 1 incl. sub-types Sub-types →
- Chester porphyria 0 trials
- Erythropoietic uroporphyria associated with myeloid malignancy 0 trials
- Porphyria due to ALA dehydratase deficiency 0 trials
Xeroderma pigmentosum 4 trials · 6 incl. sub-types
10 sub-types
- Xeroderma pigmentosum group F 1 trial
- Xeroderma pigmentosum variant type 1 trial
- Xeroderma pigmentosum group A 0 trials
- Xeroderma pigmentosum group B 0 trials
- Xeroderma pigmentosum group C 0 trials
- Xeroderma pigmentosum group D 0 trials
- Xeroderma pigmentosum group E 0 trials
- Xeroderma pigmentosum group G 0 trials
- Xeroderma pigmentosum, autosomal dominant, mild 0 trials
- Xeroderma pigmentosum, complementation group J 0 trials
Xeroderma pigmentosum-Cockayne syndrome complex 1 trial · 2 incl. sub-types
6 sub-types
- Xeroderma pigmentosum group F 1 trial
- Xeroderma pigmentosum group B 0 trials
- Xeroderma pigmentosum group D 0 trials
- Xeroderma pigmentosum group G 0 trials
- Xeroderma pigmentosum, type F/Cockayne syndrome 0 trials
- Xeroderma pigmentosum, type G/Cockayne syndrome 0 trials
Rothmund-Thomson syndrome 1 trial
4 sub-types
- Rothmund-Thomson syndrome type 1 0 trials
- Rothmund-Thomson syndrome type 2 0 trials
- Rothmund-Thomson syndrome type 3 0 trials
- Rothmund-Thomson syndrome type 4 0 trials
Bloom syndrome 0 trials
UV-sensitive syndrome 0 trials
3 sub-types
- UV-sensitive syndrome 1 0 trials
- UV-sensitive syndrome 2 0 trials
- UV-sensitive syndrome 3 0 trials

Most studied deeper sub-types

X-linked erythropoietic protoporphyria (10) Acute intermittent porphyria (5) Hereditary coproporphyria (5) Protoporphyria, erythropoietic, 1 (2) Variegate porphyria (2) Familial porphyria cutanea tarda (1) Protoporphyria, erythropoietic, 2 (1) Autosomal erythropoietic protoporphyria (0) Encephalopathy, porphyria-related (0) Harderoporphyria (0) Hepatoerythropoietic porphyria (0) Leukoencephalopathy, porphyria-related (0) Porphyria, acute intermittent, nonerythroid variant (0) Variegate porphyria, childhood-onset (0)

Including sub-types (31) Tagged with Hereditary photodermatosis (0)

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