Informaţii despre

Nume Xeroderma Pigmentosum, Variant Type
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare
Clasificari ICD10 Xeroderma pigmentosum
Clasificare anatomică Malacards Boli de piele
Boli din aceeaşi familie Xeroderma Pigmentosum, Type 2; Xeroderma Pigmentosum, Type 9

Vezi şi

Boli A-Z Acoustic Neuroma Adenocarcinoma Adie Pupil Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Amelanotic Melanoma Aminoaciduria Angiosarcoma Angiosarcoma of the Scalp Aniridia 1 Anorexia Nervosa 1 Argyria Arthrochalasia Ehlers-Danlos Syndrome Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Ataxia Neuropathy Spectrum Ataxia-Oculomotor Apraxia 3 Ataxia-Telangiectasia Autism Autosomal Recessive Disease Basal Cell Carcinoma Basal Cell Nevus Syndrome Basosquamous Carcinoma Bladder Cancer Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Bloom Syndrome Breast Cancer Burns Cataract Cerebro-Oculo-Facio-Skeletal Syndrome Cerebrooculofacioskeletal Syndrome 1 Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Cockayne Syndrome Cockayne Syndrome a Cockayne Syndrome B Cockayne Syndrome Type I Cockayne Syndrome Type Ii Cockayne Syndrome Type Iii Colorectal Cancer Congenital Short Bowel Syndrome Conjunctival Squamous Cell Carcinoma Craniosynostosis 2 De Sanctis-Cacchione Syndrome Diabetes Mellitus Diffuse Gastric Cancer Dilated Cardiomyopathy Dwarfism Dysautonomia Dyschromatosis Symmetrica Hereditaria Dyschromatosis Universalis Hereditaria 3 Dystonia Esophageal Cancer Fanconi Anemia, Complementation Group E Gastric Cancer Germ Cells Tumors Glioma Hepatic Adenomas, Familial Hepatocellular Carcinoma Herpes Simplex Idiopathic Infantile Hypercalcemia Keratoacanthoma Laryngitis Leiomyoma Lentigo Maligna Melanoma Lesch-Nyhan Syndrome Leukemia Limbal Stem Cell Deficiency Lung Cancer Melanoma Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Self-Healing Squamous Epithelioma Mutagen Sensitivity Myelodysplastic Syndrome Myiasis Myoma Nasopharyngeal Carcinoma Nasopharyngitis Nephrotic Syndrome Neuronitis Orotic Aciduria Ovarian Cancer Parkinsonism with Spasticity, X-Linked Pellagra Prostate Cancer Prostatitis Psoriasis Psoriasis 13 Rickets Right Atrial Isomerism Sarcoidosis 2 Sarcoma Serpin Peptidase Inhibitor, Clade a, Member 2, Pseudogene Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Skin Squamous Cell Carcinoma Soft Tissue Sarcoma Spasmodic Dystonia Spinal Cord Astrocytoma Spondyloocular Syndrome Sporadic Breast Cancer Squamous Cell Carcinoma Squamous Cell Carcinoma of the Oropharynx Testicular Cancer Tetraamelia Syndrome, Autosomal Recessive Three M Syndrome 1 Thrombasthenia Trichothiodystrophy 1, Photosensitive Tumor Suppressor Gene on Chromosome 11 Uv-Sensitive Syndrome Vaccinia Werner Syndrome Xeroderma Pigmentosum, Complementation Group a Xeroderma Pigmentosum, Complementation Group B Xeroderma Pigmentosum, Complementation Group C Xeroderma Pigmentosum, Complementation Group D Xeroderma Pigmentosum, Complementation Group E Xeroderma Pigmentosum, Complementation Group F Xeroderma Pigmentosum, Complementation Group G Xeroderma Pigmentosum Group E Xfe Progeroid Syndrome