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Ontology Browser

Term:
autosomal dominant keratosis follicularis spinulosa decalvans (DOID:0080755)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0) Naked Mole-rat: (0) Green Monkey: (0)
Parent Terms Term With Siblings Child Terms
alopecia areata +   
Alopecia Congenita Keratosis Palmoplantaris +   
Alopecia Contractures Dwarfism Mental Retardation 
alopecia universalis +   
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 +   
Androgenetic Alopecia 2 
Androgenetic Alopecia 3 
androgenic alopecia  
atrichia with papular lesions  
autosomal dominant keratosis follicularis spinulosa decalvans 
A keratosis follicularis spinulosa decalvans that has_material_basis_in autosomal dominant inheritance. (DO)
Bullous Dystrophy, Hereditary Macular Type 
Cancer, Alopecia, Pigment Dyscrasia, Onychodystrophy, and Keratoderma  
Central Centrifugal Cicatricial Alopecia  
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy  
chemotherapy-induced alopecia  
Congenital Alopecia X-Linked 
Cutaneous Telangiectasia and Cancer Syndrome, Familial  
dermatopathia pigmentosa reticularis  
Ectodermal Dysplasia Syndrome with Distinctive Facial Appearance and Preaxial Polydactyly of Feet 
Ectodermal Dysplasia, Alopecia, Preaxial Polydactyly 
Familial Focal Alopecia 
Follicular Hamartoma, Alopecia, Cystic Fibrosis 
follicular mucinosis 
frontal fibrosing alopecia  
frontonasal dysplasia 2  
GAPO syndrome  
Garret Tripp Syndrome 
Gomez Lopez Hernandez Syndrome 
GROWTH RESTRICTION, HYPOPLASTIC KIDNEYS, ALOPECIA, AND DISTINCTIVE FACIES  
Hypergonadotropic Hypogonadism and Partial Alopecia 
hypotrichosis 7  
hypotrichosis-lymphedema-telangiectasia-renal defect syndrome  
ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis  
IFAP Syndrome +   
Jagell Holmgren Hofer Syndrome 
Johnson Neuroectodermal Syndrome 
Kuster Majewski Hammerstein Syndrome 
loose anagen hair syndrome +   
Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis  
mandibulofacial dysostosis with alopecia  
Microcephaly Sparse Hair Mental Retardation Seizures 
Moloney Syndrome 
Neurodevelopmental Disorder with Alopecia and Brain Abnormalities  
palmoplantar keratoderma and congenital alopecia 2 
PARC Syndrome 
Patel Bixler Syndrome 
Perniola Krajewska Carnevale Syndrome 
Satoyoshi Syndrome 
Scholte Syndrome 
Slti Salem Syndrome 
T-cell immunodeficiency, congenital alopecia, and nail dystrophy  
telogen effluvium 
Thumb Deformity and Alopecia 
Thumb Deformity, Alopecia, Pigmentation Anomaly 
Urban Schosser Spohn Syndrome  
Woodhouse-Sakati syndrome  
Woolly Hair, Hypotrichosis, Everted Lower Lip and Outstanding Ears 
X-linked keratosis follicularis spinulosa decalvans  

Synonyms
Primary IDs: MESH:C567553
Alternate IDs: MIM:612843
Definition Sources: https://pubmed.ncbi.nlm.nih.gov/18984066/ "DO" "DO"

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