FTP Download
Chinchilla Research Resource Database
   
Keyword
  

Ontology Browser

Term:
Keratosis Follicularis Spinulosa Decalvans, X-Linked (DOID:9003499)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (2) Bonobo: (2) Dog: (2) Squirrel: (2)
Parent Terms Term With Siblings Child Terms
ichthyosis +     
Abruzzo Erickson Syndrome  
Absence of Fingerprints  
Achromatopsia Incomplete, X-Linked 
Acquired Ichthyosis 
Actinic Prurigo  
Agammaglobulinemia, X-Linked, Type 2 
Aicardi syndrome 
Albinism +   
Alpha-Thalassemia Myelodysplasia Syndrome  
Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis  
Alzheimer's disease 16 
androgen insensitivity syndrome +   
Anemia, X-Linked, without Thrombocytopenia 
Anencephaly and Spina Bifida X-Linked 
angioma serpiginosum +  
Anhidrotic Ectodermal Dysplasia with Immunodeficiency, Osteopetrosis, and Lymphedema  
Annular Erythema 
arterial tortuosity syndrome  
Arthrogryposis, X-Linked, Type V 
atopic dermatitis +   
Atrophia Maculosa Varioliformis Cutis, Familial 
Atypical Mycobacteriosis, Familial, X-Linked 1  
Atypical Mycobacteriosis, Familial, X-Linked 2  
AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS  
autosomal dominant keratitis-ichthyosis-deafness syndrome  
autosomal recessive congenital ichthyosis +   
Basaloid Follicular Hamartoma Syndrome, Generalized, Autosomal Dominant 
Bloch-Sulzberger syndrome +   
Bornholm Eye Disease 
Branchial Arch Syndrome X-Linked 
Bresheck/Bresek Syndrome 
bullous congenital ichthyosiform erythroderma  
Bullous Dystrophy, Hereditary Macular Type 
Buschke-Ollendorff Syndrome  
Camptodactyly-Ichthyosis Syndrome 
Cardiac Valvular Dysplasia, X-Linked  
cataract 40  
Cataract and Congenital Ichthyosis 
CEREBRAL-CEREBELLAR-COLOBOMA SYNDROME, X-LINKED  
CHILD Syndrome  
Chondrodysplasia with Platyspondyly, Distinctive Brachydactyly, Hydrocephaly, and Microphthalmia  
Choroideremia +   
chromosome Xp11.23-p11.22 duplication syndrome 
Chromosome Xq28 Duplication Syndrome 
Cleft Palate with Ankyloglossia  
Collagenosis, Familial Reactive Perforating 
combined T cell and B cell immunodeficiency +   
Cone Dystrophy, X-Linked, with Tapetal-like Sheen 
Congenital Adrenal Hypoplasia with Precocious Puberty  
Congenital Alopecia X-Linked 
Congenital Erythroderma with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-IgE  
Congenital Heart Defects, X-Linked +   
congenital hypogammaglobulinemia 
Congenital Ichthyosis with Trichothiodystrophy +   
Congenital Idiopathic Intestinal Pseudoobstruction  
Congenital Myopathy, with Fiber-Type Disproportion, X-Linked 
Congenital Ptosis, Hereditary 2 
Cornelia De Lange Syndrome 2  
Cornelia De Lange Syndrome 5  
Corpus Callosum, Partial Agenesis of, X-Linked  
Craniofacioskeletal Syndrome 
Cutaneous Bullous Amyloidosis 
cutaneous porphyria  
cutis laxa +   
Danon disease  
Deafness, High-Frequency Sensorineural, X-Linked  
Deafness, X-Linked 1  
Deafness, X-Linked 3 
Deafness, X-Linked 4  
Deafness, X-Linked 5  
deafness-intellectual disability, Martin-Probst type syndrome  
Deal Barratt Dillon Syndrome 
Dilated Cardiomyopathy 3A  
Distal Arthrogryposis Multiplex Congenita, X-Linked  
Dowling-Degos disease +   
Dykes Markes Harper Syndrome 
dyschromatosis universalis hereditaria +   
Dyserythropoietic Anemia with Thrombocytopenia  
dyskeratosis congenita +   
early infantile epileptic encephalopathy 8  
early infantile epileptic encephalopathy 9  
Early Onset Parkinsonism with Mental Retardation  
ectodermal dysplasia +   
Ectodermal Dysplasia 1, Anhidrotic +   
Ehlers-Danlos syndrome +   
Ehlers-Danlos Syndrome Type 5 
Epidermodysplasia Verruciformis, X-Linked 
epidermolysis bullosa +   
Episodic Muscle Weakness, X-Linked 
erythrokeratodermia variabilis +   
Erythrokeratodermia with Ataxia  
Erythropoietic Protoporphyria, X-Linked Dominant  
Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa of Siemens-like  
External Ophthalmoplegia and Myopia 
Fabry disease +   
Familial Exudative Vitreoretinopathy, X-Linked Recessive  
favism  
Fetal Akinesia Syndrome, X-Linked 
Fg Syndrome 5 
Follicular Atrophoderma, Perioral Pigmented, with Milia and Epidermoid Cysts 
Gerodermia Osteodysplastica  
glycogen storage disease VIII 
Grover's Disease 
Hailey-Hailey disease  
Hepatic Porphyrias +   
Hereditary Autoinflammatory Diseases +   
hereditary mucosal leukokeratosis  
HID Syndrome  
Histiocytic Dermatoarthritis 
Hodgkin Disease, X-Linked Pseudoautosomal 
Hyaluronan Metabolism, Defect in 
Hydrocephalus with Cerebellar Agenesis 
Hypertrichosis Congenital Generalized X-Linked 
Hypogammaglobulinemia, X-Linked  
Hypohidrotic Ectodermal Dysplasia, with Immune Deficiency  
Hypoparathyroidism, X-Linked 
Hypospadias 1, X-Linked  
Hypospadias 2, X-Linked  
Ichthyosis Cheek Eyebrow Syndrome 
Ichthyosis Exfoliativa  
Ichthyosis Follicularis Atrichia Photophobia Syndrome  
Ichthyosis Hystrix Gravior 
Ichthyosis Hystrix, Curth Macklin Type  
Ichthyosis Prematurity Syndrome  
Ichthyosis Tapered Fingers Midline Groove Up 
ichthyosis vulgaris +   
Ichthyosis, Mental Retardation, Dwarfism, and Renal Impairment 
Ichthyosis, Spastic Quadriplegia, and Mental Retardation  
Ichthyosis, Split Hairs, and Amino Aciduria 
Ichthyosis-Mental Retardation Syndrome with Large Keratohyalin Granules in the Skin 
Idiopathic Short Stature, X-Linked  
Intracranial Berry Aneurysm 5 
Isolated Noncompaction of the Ventricular Myocardium +   
Isolated Osteopoikilosis 
Jagell Holmgren Hofer Syndrome 
Juvenile Spring Eruption of Ears 
Keratolytic Winter Erythema  
keratosis follicularis +   
Keratosis Follicularis Spinulosa Decalvans, X-Linked  
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma  
Koone Rizzo Elias Syndrome 
Leigh Syndrome, X-Linked  
Leukoencephalopathy with Metaphyseal Chondrodysplasia 
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis 
LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 3  
lipoid proteinosis  
Liver Glycogenosis, X-Linked, Type II 
Macular Dystrophy, X-Linked +   
major affective disorder 2 
megalocornea +   
Membranoproliferative Glomerulonephritis, X-Linked 
MEND SYNDROME  
Mental Retardation, Skeletal Dysplasia, and Abducens Palsy 
Mental Retardation, X-Linked +   
Microcephaly Microcornea Syndrome Seemanova Type 
Microphthalmia, Isolated, with Coloboma 1 
Microphthalmia, Syndromic 7  
Midline Defects, X-Linked 
monilethrix +   
Muir-Torre syndrome  
Multiple Noduli Cutanei with Urinary Tract Abnormalities 
Multiple Pterygium Syndrome, X-Linked 
Myopathy, Reducing Body, X-Linked, Childhood-Onset  
Myopathy, Reducing Body, X-Linked, Early-Onset, Severe  
Myopia 1 
Myopia 13 
MYOPIA 26, X-LINKED, FEMALE-LIMITED  
Nasodigitoacoustic Syndrome  
NEMO Mutation with Immunodeficiency 
Nephrogenic Syndrome of Inappropriate Antidiuresis  
Nephrolithiasis, X-Linked Recessive, with Renal Failure  
Neu-Laxova syndrome 1  
Neural Tube Defects X-Linked 
Nisch syndrome  
Nystagmus 1, Congenital, X- Linked  
Nystagmus 5, Infantile Periodic Alternating 
Oculotrichodysplasia 
Opitz GBBB Syndrome, Type I  
Optic Atrophy 2 
ornithine carbamoyltransferase deficiency  
orofaciodigital syndrome IX  
Osteosclerosis with Ichthyosis and Fractures 
ovarian dysgenesis 2  
palmoplantar keratosis +   
Panhypopituitarism X-Linked  
Parana Hard Skin Syndrome 
Parkinson's Disease 12 
Pedal Onychogryposis with Keratosis Plantaris and Coarse Hair 
peeling skin syndrome +   
Perifolliculitis Capitis Abscedens Et Suffodiens, Familial 
Periventricular Nodular Heterotopia 4  
Periventricular Nodular Heterotopia, with Frontometaphyseal Dysplasia 
Phosphoglycerate Kinase 1 Deficiency  
Plasminogen Deficiency, Type I  
Poikiloderma, Hereditary Sclerosing +   
porokeratosis +   
Premature Ovarian Failure 2a  
primary cutaneous amyloidosis  
Primary Localized Cutaneous Amyloidosis, 2  
Primary Localized Cutaneous Amyloidosis, 3  
Progressive Hearing Loss Stapes Fixation  
Progressive Muscular Dystrophy, Pectorodorsal 
Progressive Osseous Heteroplasia  
Progressive Vitiligo with Mental Retardation and Urethral Duplication 
Prolidase Deficiency  
Properdin Deficiency, Type II  
Properdin Deficiency, Type III  
Properdin Deficiency, X-Linked  
Prostate Cancer, Hereditary, X-Linked 1 
Prostate Cancer, Hereditary, X-Linked 2 
Proud Syndrome  
pseudoxanthoma elasticum +   
Radial Ray Deficiency, X-Linked 
Radiation Sensitivity of Natural Killer Activity 
Radius Absent Anogenital Anomalies 
Reticulate Pigmentary Disorder, with Systemic Manifestations  
Reticuloendotheliosis, X-Linked 
retinitis pigmentosa 3  
retinitis pigmentosa 34 
retinitis pigmentosa 6 
Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked  
Rothmund-Thomson syndrome +   
Rud Syndrome 
Russell-Silver Syndrome, X-Linked 
Ruzicka Goerz Anton syndrome 
Sammartino De Crecchio Syndrome 
Selective Tooth Agenesis, X-Linked, 1  
Severe Congenital Neutropenia, X-Linked  
Sjogren-Larsson syndrome +   
Sketetal Dysplasia Coarse Facies Mental Retardation 
Skin Fragility-Woolly Hair Syndrome  
Spina Bifida, X-Linked 
Spinal Muscular Atrophy, Distal, X-Linked 3  
Spinocerebellar Ataxia, X-Linked 1  
Spinocerebellar Ataxia, X-Linked 5 
Spinocerebellar Ataxia, X-Linked, 3 
split hand-foot malformation 2 
Spondyloepimetaphyseal Dysplasia, X-Linked  
Spondylometaphyseal Dysplasia, X-Linked 
Stiff Skin Syndrome  
Storm Syndrome 
Stormorken syndrome  
Surfactant Metabolism Dysfunction, Pulmonary, 4  
syndromic X-linked intellectual disability Turner type  
Systemic Hyalinosis  
Terminal Osseous Dysplasia and Pigmentary Defects  
Testicular Germ Cell Tumor 1 
Thrombocytopenia 1  
Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis  
Thrombocytopenia, X-Linked, Intermittent  
Thrombocytosis, Familial X-Linked 
Thyroxine-Binding Globulin Deficiency +   
Torticollis Keloids Cryptorchidism Renal Dysplasia 
Trichodysplasia-Xeroderma 
Trichothiodystrophy Syndromes +   
VACTERL/VATER Association with Hydrocephalus  
Vasquez Hurst Sotos Syndrome 
Vohwinkel Syndrome, Variant Form  
Von Willebrand Disease, X-Linked Form 
Wells Jankovic Syndrome 
X Inactivation, Familial Skewed, 1  
X Inactivation, Familial Skewed, 2 
X-Linked Anemia with or without Neutropenia and/or Platelet Abnormalities  
X-linked cleft palate with or without ankyloglossia  
X-linked cone-rod dystrophy 1  
X-linked cone-rod dystrophy 2 
X-linked dilated cardiomyopathy  
X-linked dominant disease +   
X-Linked Epilepsy, with Variable Learning Disabilities and Behavior Disorders  
X-linked hereditary ataxia +   
X-Linked Hydrocephalus +   
X-linked ichthyosis +   
X-Linked Immunodeficiency with Deficiency of 115,000 Dalton Surface Glycoprotein 
X-Linked Modifier for Neurofunctional Defects 
X-linked nonsyndromic deafness +   
X-linked recessive disease +   
X-Linked Retinitis Pigmentosa, and Sinorespiratory Infections, with or without Deafness  
X-Linked Tetra-Amelia 
X-Linked Thrombocytopenia, with or without Dyserythropoietic Anemia  
X-Linked Thrombophilia, due to Factor IX Defect  
X-Linked Vesicoureteral Reflux 
xeroderma of eyelid 
xeroderma pigmentosum +   
Zunich Neuroectodermal Syndrome  

Synonyms
Exact Synonyms: Keratosis follicularis spinulosa decalvans ;   Keratosis follicularis spinulosa decalvans cum ophiasi ;   Kfsdx
Primary IDs: MESH:C536159 ;   RDO:0001624
Alternate IDs: OMIM:308800

paths to the root