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adenosquamous carcinoma +
Aerodigestive Tract Squamous Cell Carcinoma +
Alopecia Congenita Keratosis Palmoplantaris +
Alopecia Contractures Dwarfism Mental Retardation
Alopecia Universalis, Onychodystrophy, Vitiligo
Alopecia, Epilepsy, Pyorrhea, Mental Subnormality
Alopecia, Hypogonadism, Extrapyramidal Disorder
alopecia, neurologic defects, and endocrinopathy syndrome
Alopecia-Epilepsy-Oligophrenia Syndrome of Moynahan
alopecia-mental retardation syndrome +
Ameloonychohypohidrotic Syndrome
anal canal squamous cell carcinoma
anal margin squamous cell carcinoma
anal squamous cell carcinoma +
Anonychia Onychodystrophy
Anonychia with Flexural Pigmentation
atrichia with papular lesions
autosomal dominant congenital deafness with onychodystrophy
autosomal dominant keratosis follicularis spinulosa decalvans
basaloid squamous cell carcinoma +
bladder squamous cell carcinoma +
bladder urachal squamous cell carcinoma
Bloch-Sulzberger syndrome +
bone squamous cell carcinoma
Brachymorphism-Onychodysplasia-Dysphalangism Syndrome
breast squamous cell carcinoma +
Bullous Dystrophy, Hereditary Macular Type
Cancer, Alopecia, Pigment Dyscrasia, Onychodystrophy, and Keratoderma CAPOK syndrome is characterized by onset of symptoms in the first year of life, with the development of progressive alopecia, hypo- and hyperpigmented macular skin lesions, palmoplantar keratoderma, and nail dystrophy. Beginning in the third decade of life, patients develop recurrent squamous cell carcinomas. Some patients may have brittle teeth resulting in tooth loss, and multinodular goiter has been observed. CAPOK can be caused by homozygous mutation in the SASH1 gene on chromosome 6q24. (OMIM)
Cartwright Nelson Fryns Syndrome
Central Centrifugal Cicatricial Alopecia
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
cervical squamous cell carcinoma +
chemotherapy-induced alopecia
colon squamous cell carcinoma
Congenital Alopecia X-Linked
Congenital Erythroderma with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-IgE
conjunctival pigmentation
conjunctival squamous cell carcinoma
cornea squamous cell carcinoma
Corneodermatoosseous Syndrome
Curly Hair-Acral Keratoderma-Caries Syndrome
Curly Hair-Ankyloblepharon-Nail Dysplasia Syndrome
Cutaneous Telangiectasia and Cancer Syndrome, Familial
dermatopathia pigmentosa reticularis
Diffuse Palmoplantar Keratoderma +
Double Nail for Fifth Toe
dyschromatosis symmetrica hereditaria
dyschromatosis universalis hereditaria +
Ectodermal Dysplasia Syndrome with Distinctive Facial Appearance and Preaxial Polydactyly of Feet
Ectodermal Dysplasia, Alopecia, Preaxial Polydactyly
endometrial squamous cell carcinoma +
esophagus squamous cell carcinoma +
ethmoid sinus squamous cell carcinoma
external ear squamous cell carcinoma
fallopian tube squamous cell carcinoma
Fitzsimmons-McLachlan-Gilbert syndrome
Focal Palmoplantar and Gingival Keratosis
Follicular Hamartoma, Alopecia, Cystic Fibrosis
frontal fibrosing alopecia
frontal sinus squamous cell carcinoma
gallbladder squamous cell carcinoma
Gomez Lopez Hernandez Syndrome
Gorlin Bushkell Jensen Syndrome
Grouped Pigmentation of the Macula
GROWTH RESTRICTION, HYPOPLASTIC KIDNEYS, ALOPECIA, AND DISTINCTIVE FACIES
head and neck squamous cell carcinoma +
Hypergonadotropic Hypogonadism and Partial Alopecia
Hyperkeratosis-Hyperpigmentation Syndrome
Hypospadias-Mental Retardation Syndrome
hypotrichosis-lymphedema-telangiectasia-renal defect syndrome
Hypotrichosis-Osteolysis-Periodontitis-Palmoplantar Keratoderma Syndrome
ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis
inflammatory poikiloderma with hair abnormalities and acral keratoses
Jagell Holmgren Hofer Syndrome
Johnson Neuroectodermal Syndrome
Judge Misch Wright Syndrome
keratinizing squamous cell carcinoma
Keratoderma Palmoplantaris Transgrediens
Keratoderma-Ichthyosis-Deafness Syndrome, Autosomal Recessive
Keratosis Palmaris et Plantaris with Clinodactyly
keratosis palmoplantaris striata +
Kuster Majewski Hammerstein Syndrome
lacrimal gland squamous cell carcinoma
laryngeal squamous cell carcinoma +
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis
loose anagen hair syndrome +
lung squamous cell carcinoma +
Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis
Macules Hereditary Congenital Hypopigmented and Hyperpigmented
Mammary-Digital-Nail Syndrome
mandibulofacial dysostosis with alopecia
maxillary sinus squamous cell carcinoma
Microcephaly Sparse Hair Mental Retardation Seizures
middle ear squamous cell carcinoma
mutilating palmoplantar keratoderma with periorificial keratotic plaques +
Naegeli-Franceschetti-Jadassohn syndrome
Neurodevelopmental Disorder with Alopecia and Brain Abnormalities
nonepidermolytic palmoplantar keratoderma +
nonsyndromic congenital nail disorder +
Oculocerebral Hypopigmentation Syndrome Type Preus
ONYCHODYSTROPHY, OSTEODYSTROPHY, IMPAIRED INTELLECTUAL DEVELOPMENT, AND SEIZURES SYNDROME
Onychotrichodysplasia and Neutropenia
Otoonychoperoneal Syndrome
ovarian squamous cell carcinoma
Palmoplantar Hyperkeratosis and True Hermaphroditism
Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and Sex Reversal
palmoplantar keratoderma and congenital alopecia 2
PALMOPLANTAR KERATODERMA AND WOOLLY HAIR +
Palmoplantar Keratoderma, Nagashima Type
Palmoplantar Keratoderma, Norrbotten Recessive Type
Palmoplantar Keratoderma, Spastic Paralysis
palmoplantar keratoderma-deafness syndrome
palmoplantar keratoderma-esophageal carcinoma syndrome
pancreatic squamous cell carcinoma
papillary squamous carcinoma
Papillon-Lefevre disease +
penis squamous cell carcinoma +
Perniola Krajewska Carnevale Syndrome
pharynx squamous cell carcinoma +
Pigmented Purpuric Eruption
Pili Torti Onychodysplasia
Pinheiro Freire-Maia Miranda Syndrome
Porokeratosis 2, Palmar, Plantar, and Disseminated Type
Powell Venencie Gordon syndrome
Precocious Graying of Hair
prostate squamous cell carcinoma
punctate palmoplantar keratoderma +
rectum squamous cell carcinoma +
Red Skin Pigment Anomaly of New Guinea
renal pelvis squamous cell carcinoma
Russell-Silver Syndrome, X-Linked
Schinzel Giedion syndrome
Schopf-Schulz-Passarge syndrome
scrotum squamous cell carcinoma
Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis
skin squamous cell carcinoma +
Skin/Hair/Eye Pigmentation, Variation In, 1
Skin/Hair/Eye Pigmentation, Variation In, 10
Skin/Hair/Eye Pigmentation, Variation In, 11
SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 2
Skin/Hair/Eye Pigmentation, Variation In, 3
Skin/Hair/Eye Pigmentation, Variation In, 4
Skin/Hair/Eye Pigmentation, Variation In, 5
Skin/Hair/Eye Pigmentation, Variation In, 6
Skin/Hair/Eye Pigmentation, Variation In, 7
Skin/Hair/Eye Pigmentation, Variation In, 8
sphenoid sinus squamous cell carcinoma
squamous cell bile duct carcinoma +
Steatocystoma Multiplex with Natal Teeth
Stern Lubinsky Durrie Syndrome
stromal corneal pigmentation
subglottis squamous cell carcinoma +
supraglottis squamous cell carcinoma +
T-cell immunodeficiency, congenital alopecia, and nail dystrophy
Temple-Baraitser syndrome
terminal osseous dysplasia
Thumb Deformity and Alopecia
Thumb Deformity, Alopecia, Pigmentation Anomaly
thymus squamous cell carcinoma +
Total Anonychia with Microcephaly
Ulnar Hypoplasia with Mental Retardation
Urban Schosser Spohn Syndrome
ureter squamous cell carcinoma
urethra squamous cell carcinoma +
vulva squamous cell carcinoma +
Waardenburg Syndrome Type 4 +
White Forelock with Malformations
Woodhouse-Sakati syndrome
Woolly Hair, Hypotrichosis, Everted Lower Lip and Outstanding Ears
X-linked reticulate pigmentary disorder
Zori Stalker Williams Syndrome
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