Palmoplantar Keratoderma-Xx Sex Reversal-Predisposition To Squamous Cell Carcinoma Syndrome |
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Squamous cell carcinoma of the skin, Palmoplantar keratoderma |
ORPHA:85112 |
Epidermodysplasia Verruciformis, Susceptibility To, 2 |
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Verruca plana, Squamous cell carcinoma of the skin |
OMIM:618231 |
Cutaneous Neuroendocrine Carcinoma |
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Neoplasm of the outer ear, Squamous cell carcinoma of the skin, Merkel cell skin cancer, Carcinoi... |
ORPHA:79140 |
Familial Multinodular Goiter |
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Sertoli cell neoplasm, Pleuropulmonary blastoma, Alveolar rhabdomyosarcoma, Thyroid carcinoma, Pi... |
ORPHA:276399 |
Huriez Syndrome |
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Squamous cell carcinoma of the skin, Congenital palmoplantar hyperkeratosis |
OMIM:181600 |
Pilomatrixoma |
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Pilomatrixoma |
OMIM:132600 |
Apc-Related Attenuated Familial Adenomatous Polyposis |
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Osteoma, Fibrosarcoma, Desmoid tumors, Adrenocortical adenoma, Medulloblastoma, Multiple gastric ... |
ORPHA:247806 |
Gardner Syndrome |
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Colon cancer, Ampulla of Vater carcinoma, Hepatoblastoma, Brain neoplasm, Osteoma, Fibrosarcoma, ... |
ORPHA:79665 |
Epidermodysplasia Verruciformis, Susceptibility To, 5 |
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Squamous cell carcinoma of the skin, Verrucae |
OMIM:618309 |
Mosaic Variegated Aneuploidy Syndrome 7 With Inflammation And Tumor Predisposition |
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Pilomatrixoma, Embryonal rhabdomyosarcoma, Cervix cancer, Adenocarcinoma of the colon, Lipoma, Mu... |
OMIM:620189 |
Pilomatrixoma |
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Neoplasm of head and neck, Pilomatrixoma |
ORPHA:91414 |
Oculocutaneous Albinism Type 1A |
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Basal cell carcinoma, Squamous cell carcinoma of the skin, Hyperkeratosis |
ORPHA:79431 |
Turcot Syndrome With Polyposis |
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Glioma, Hepatoblastoma, Brain neoplasm, Desmoid tumors, Leukemia, Basal cell carcinoma, Glioblast... |
ORPHA:99818 |
Xeroderma Pigmentosum, Complementation Group E |
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Basal cell carcinoma, Squamous cell carcinoma of the skin, Melanoma |
OMIM:278740 |
Disabling Pansclerotic Morphea Of Childhood |
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Squamous cell carcinoma of the skin |
OMIM:620443 |
Xeroderma Pigmentosum, Complementation Group C |
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Basal cell carcinoma, Squamous cell carcinoma of the skin, Actinic keratosis, Cutaneous melanoma |
OMIM:278720 |
Oculocutaneous Albinism Type 1B |
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Basal cell carcinoma, Squamous cell carcinoma of the skin, Melanoma |
ORPHA:79434 |
Pulmonary Fibrosis And/Or Bone Marrow Failure Syndrome, Telomere-Related, 7 |
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Squamous cell carcinoma of the skin, Myelodysplasia |
OMIM:620365 |
Xeroderma Pigmentosum, Complementation Group B |
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Basal cell carcinoma, Squamous cell carcinoma of the skin, Neoplasm, Cutaneous melanoma |
OMIM:610651 |
Dyskeratosis Congenita, Digenic |
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Basal cell carcinoma, Melanoma, Squamous cell carcinoma of the skin |
OMIM:620040 |
Xeroderma Pigmentosum, Complementation Group A |
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Melanoma, Squamous cell carcinoma of the skin |
OMIM:278700 |
Hermansky-Pudlak Syndrome |
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Basal cell carcinoma, Squamous cell carcinoma of the skin, Hyperkeratosis |
ORPHA:79430 |
Xeroderma Pigmentosum-Cockayne Syndrome Complex |
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Basal cell carcinoma, Melanoma, Squamous cell carcinoma of the skin |
ORPHA:220295 |
Oculocutaneous Albinism Type 2 |
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Basal cell carcinoma, Squamous cell carcinoma of the skin, Cutaneous melanoma |
ORPHA:79432 |
Autosomal Dominant Generalized Epidermolysis Bullosa Simplex, Severe Form |
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Squamous cell carcinoma of the skin, Palmoplantar keratoderma |
ORPHA:79396 |
Lmna-Related Cardiocutaneous Progeria Syndrome |
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Basal cell carcinoma, Squamous cell carcinoma of the skin, Papillary renal cell carcinoma, Pulmon... |
ORPHA:363618 |
Dyskeratosis Congenita, Autosomal Dominant 1 |
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Squamous cell carcinoma of the skin, Myelodysplasia |
OMIM:127550 |
Rubinstein-Taybi Syndrome Due To 16P13.3 Microdeletion |
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Neoplasm, Spinal cord tumor, Pilomatrixoma, Meningioma |
ORPHA:353281 |
Tetrasomy 9P |
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Pilomatrixoma |
ORPHA:3310 |
Rubinstein-Taybi Syndrome Due To Ep300 Haploinsufficiency |
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Pilomatrixoma, Meningioma |
ORPHA:353284 |
Rubinstein-Taybi Syndrome Due To Crebbp Mutations |
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Pilomatrixoma, Meningioma |
ORPHA:353277 |