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Term:
Basaloid Follicular Hamartoma Syndrome, Generalized, Autosomal Dominant
(DOID:9008314)
Annotations:
Rat: (0)
Mouse: (0)
Human: (0)
Chinchilla: (0)
Bonobo: (0)
Dog: (0)
Squirrel: (0)
Pig: (0)
Parent Terms
Term With Siblings
Child Terms
Genetic Skin Diseases
+
Hamartoma
+
Actinic Prurigo
adermatoglyphia
Albinism
+
Annular Erythema
arterial tortuosity syndrome
atopic dermatitis
+
Atrophia Maculosa Varioliformis Cutis, Familial
Autoinflammation with Arthritis and Dyskeratosis
autosomal recessive congenital ichthyosis
+
Basaloid Follicular Hamartoma Syndrome, Generalized, Autosomal Dominant
Bloch-Sulzberger syndrome
+
bullous congenital ichthyosiform erythroderma
Buschke-Ollendorff syndrome
cherubism
+
Collagenosis, Familial Reactive Perforating
Congenital Erythroderma with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-IgE
congenital heart defects, hamartomas of tongue, and polysyndactyly
Congenital Symmetric Circumferential Skin Creases
+
Cutaneous Bullous Amyloidosis
cutaneous porphyria
cutis laxa
+
Defect in Hyaluronan Metabolism
Dowling-Degos disease
+
dyschromatosis universalis hereditaria
+
dyskeratosis congenita
+
ectodermal dysplasia
+
Ehlers-Danlos syndrome
+
epidermolysis bullosa
+
epidermolytic hyperkeratosis
+
erythrokeratodermia variabilis
+
Erythrokeratodermia with Ataxia
Follicular Hamartoma, Alopecia, Cystic Fibrosis
geroderma osteodysplasticum
Giant Mammary Hamartoma
Hailey-Hailey disease
Hamartoma, Precalcaneal Congenital Fibrolipomatous
Hamartomatous Lip
Hepatic Porphyrias
+
Hereditary Autoinflammatory Diseases
+
hereditary mucosal leukokeratosis
Hereditary Sclerosing Poikiloderma
+
Histiocytic Dermatoarthritis
hyaline fibromatosis syndrome
ichthyosis vulgaris
+
Isolated Osteopoikilosis
Juvenile Spring Eruption of Ears
Keratolytic Winter Erythema
keratosis follicularis
+
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis
lipoid proteinosis
Microgastria Limb Reduction Defect
monilethrix
+
Muir-Torre syndrome
Multiple Noduli Cutanei with Urinary Tract Abnormalities
Oculotrichodysplasia
orofaciodigital syndrome IX
Pallister-Hall syndrome
+
Pallister-Hall-like Syndrome
palmoplantar keratosis
+
Parana Hard Skin Syndrome
Pedal Onychogryposis with Keratosis Plantaris and Coarse Hair
peeling skin syndrome
+
Perifolliculitis Capitis Abscedens Et Suffodiens, Familial
Perioral Pigmented Follicular Atrophoderma with Milia and Epidermoid Cysts
plasminogen deficiency type I
poikiloderma with neutropenia
porokeratosis
+
primary cutaneous amyloidosis
+
progressive osseous heteroplasia
Progressive Vitiligo with Mental Retardation and Urethral Duplication
prolidase deficiency
pseudoxanthoma elasticum
+
PTEN hamartoma tumor syndrome
+
Rothmund-Thomson syndrome
+
Sjogren-Larsson syndrome
+
Skin Fragility-Woolly Hair Syndrome
stiff skin syndrome
Storm Syndrome
trichothiodystrophy
+
tuberous sclerosis
+
Vohwinkel Syndrome, Variant Form
X-linked ichthyosis
+
X-linked reticulate pigmentary disorder
xeroderma pigmentosum
+
Synonyms
Primary IDs:
MESH:C565284
; RDO:0013965