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Term:
Pedal Onychogryposis with Keratosis Plantaris and Coarse Hair (DOID:9001641)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0)
Parent Terms Term With Siblings Child Terms
hair disease +     
nail disease +     
Absence of Fingerprints  
Actinic Prurigo  
Al Gazali Hirschsprung Syndrome 
Albinism +   
Annular Erythema 
anonychia congenita +   
arterial tortuosity syndrome  
atopic dermatitis +   
Atrophia Maculosa Varioliformis Cutis, Familial 
AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS  
autosomal recessive congenital ichthyosis +   
Bamforth-Lazarus syndrome  
Basaloid Follicular Hamartoma Syndrome, Generalized, Autosomal Dominant 
Basaran Yilmaz Syndrome  
Bird Headed Dwarfism Montreal Type 
Bjornstad syndrome  
Bloch-Sulzberger syndrome +   
Brachycephaly, Trichomegaly, and Developmental Delay  
Brachydactyly Type A5 Nail Dysplasia 
bullous congenital ichthyosiform erythroderma  
Buschke-Ollendorff Syndrome  
candidal paronychia 
Catatrichy 
chronic mucocutaneous candidiasis +   
Collagenosis, Familial Reactive Perforating 
Congenital Erythroderma with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-IgE  
Congenital Hereditary Endothelial Dystrophy with Nail Hypoplasia 
Congenital Woolly Hair +   
Copper Deficiency, Familial Benign 
Curly Hair-Ankyloblepharon-Nail Dysplasia Syndrome  
Cutaneous Bullous Amyloidosis 
cutaneous porphyria  
cutis laxa +   
Dermatopathia Pigmentosa Reticularis  
Dermoodontodysplasia 
dilated cardiomyopathy with woolly hair and keratoderma +   
Double Nail for Fifth Toe 
Dowling-Degos disease +   
dyschromatosis universalis hereditaria +   
dyskeratosis congenita +   
ectodermal dysplasia +   
Ectodermal Dysplasia 4, Hair/Nail Type  
Ectodermal Dysplasia 9, Hair/Nail Type  
Ehlers-Danlos syndrome +   
epidermolysis bullosa +   
Epidermolysis Bullosa Simplex with Nail Dystrophy  
Epidermolysis Bullosa, Late-Onset Localized Junctional, with Mental Retardation 
erythrokeratodermia variabilis +   
Erythrokeratodermia with Ataxia  
Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa of Siemens-like  
FLOTCH Syndrome 
Follicular Atrophoderma, Perioral Pigmented, with Milia and Epidermoid Cysts 
folliculitis +   
Gerodermia Osteodysplastica  
Hailey-Hailey disease  
Hairy Palms and Soles 
Hepatic Porphyrias +   
Hereditary Autoinflammatory Diseases +   
hereditary mucosal leukokeratosis  
Hirsutism +   
Histiocytic Dermatoarthritis 
Hooft Disease 
Hyaluronan Metabolism, Defect in 
hypertrichosis +   
hypotrichosis +   
ichthyosis vulgaris +   
Isolated Osteopoikilosis 
Judge Misch Wright Syndrome 
Juvenile Spring Eruption of Ears 
Kaler Garrity Stern Syndrome 
Katsantoni Papadakou Lagoyanni Syndrome 
Keratolytic Winter Erythema  
keratosis follicularis +   
Keratosis Follicularis Spinulosa Decalvans, X-Linked  
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma  
Kozlowski-Krajewska Syndrome 
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis 
Leukonychia Totalis +   
lipoid proteinosis  
Martinez Monasterio Pinheiro Syndrome 
Menkes disease +   
monilethrix +   
Muir-Torre syndrome  
Multiple Noduli Cutanei with Urinary Tract Abnormalities 
nail-patella syndrome +   
Nails, Ingrown 
Naxos Disease  
nonsyndromic congenital nail disorder 1 
nonsyndromic congenital nail disorder 10  
nonsyndromic congenital nail disorder 2 
nonsyndromic congenital nail disorder 3  
nonsyndromic congenital nail disorder 4  
nonsyndromic congenital nail disorder 5 
nonsyndromic congenital nail disorder 6 
nonsyndromic congenital nail disorder 7 
nonsyndromic congenital nail disorder 8  
Oculotrichodysplasia 
Odontomicronychial Dysplasia 
Onycholysis +   
orofaciodigital syndrome IX  
pachyonychia congenita +   
Palmoplantar Keratoderma, Spastic Paralysis 
palmoplantar keratosis +   
Parana Hard Skin Syndrome 
paronychia 
Patel Bixler Syndrome 
Pectus Excavatum, Macrocephaly, Short Stature, Dysplastic Nails 
Pedal Onychogryposis with Keratosis Plantaris and Coarse Hair 
peeling skin syndrome +   
Perifolliculitis Capitis Abscedens Et Suffodiens, Familial 
Photosensitive Trichothiodystrophy 1  
Pili Annulati 
Pili Multigemini 
Pili Torti +  
Plasminogen Deficiency, Type I  
Poikiloderma, Hereditary Sclerosing +   
porokeratosis +   
primary cutaneous amyloidosis  
Primary Localized Cutaneous Amyloidosis, 2  
Primary Localized Cutaneous Amyloidosis, 3  
Progressive Osseous Heteroplasia  
Progressive Vitiligo with Mental Retardation and Urethral Duplication 
Prolidase Deficiency  
Pseudofolliculitis Barbae  
Pseudomonilethrix 
pseudoxanthoma elasticum +   
Reticulate Pigmentary Disorder, with Systemic Manifestations  
Rodrigues Blindness 
Rothmund-Thomson syndrome +   
Sjogren-Larsson syndrome +   
Skin Fragility-Woolly Hair Syndrome  
Stiff Skin Syndrome  
Storm Syndrome 
Subungual Exostoses 
superficial mycosis +  
Systemic Hyalinosis  
T-cell immunodeficiency, congenital alopecia, and nail dystrophy  
tinea capitis +  
tinea favosa 
tinea unguium 
Tricho-Dento-Osseous Syndrome  
Tricho-Dento-Osseous Syndrome 1 
Trichodysplasia-Xeroderma 
Trichohepatoenteric Syndrome  
Trichohepatoenteric Syndrome 2  
TRICHOMEGALY  
Trichoodontoonychial Dysplasia 
trichorhinophalangeal syndrome type I  
trichorhinophalangeal syndrome type III  
Trichostasis Spinulosa 
Trichothiodystrophy Syndromes +   
Uncombable Hair Syndrome +   
Vohwinkel Syndrome, Variant Form  
White Forelock with Malformations 
Woolly Hair, Autosomal Recessive +   
X-linked ichthyosis +   
xeroderma pigmentosum +   
yellow nail syndrome +  

Synonyms
Primary IDs: MESH:C563506
Alternate IDs: RDO:0012747

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