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Term:
dilated cardiomyopathy with woolly hair and keratoderma (DOID:0090128)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1)
Parent Terms Term With Siblings Child Terms
3-M syndrome +   
3-methylglutaconic aciduria type 5  
3MC syndrome +   
ABCD syndrome  
aceruloplasminemia  
achalasia microcephaly syndrome 
acheiropody  
achondrogenesis type IB  
achromatopsia 2  
achromatopsia 3  
achromatopsia 7  
acrocapitofemoral dysplasia  
acromesomelic dysplasia, Grebe type  
acromesomelic dysplasia, Hunter-Thompson type  
acromesomelic dysplasia, Maroteaux type  
adult spinal muscular atrophy  
agenesis of the corpus callosum with peripheral neuropathy  
Alopecia Congenita Keratosis Palmoplantaris +   
alpha-2-plasmin inhibitor deficiency  
Alstrom syndrome  
amelogenesis imperfecta hypomaturation type 2A2  
amelogenesis imperfecta hypomaturation type 2A3  
amelogenesis imperfecta hypomaturation type 2A4  
amelogenesis imperfecta hypomaturation type 2A5  
amelogenesis imperfecta type 1C  
amelogenesis imperfecta type 1F  
amelogenesis imperfecta type 1G  
amelogenesis imperfecta type 1H  
amelogenesis imperfecta type 2A1  
Antley-Bixler syndrome +   
ARC syndrome  
arrhythmogenic right ventricular dysplasia 11  
asphyxiating thoracic dystrophy +   
Athabaskan brainstem dysgenesis syndrome  
atrichia with papular lesions  
autoimmune lymphoproliferative syndrome type 2B  
autoimmune lymphoproliferative syndrome type 3  
autosomal recessive Alport syndrome  
autosomal recessive cerebellar ataxia +   
autosomal recessive chronic granulomatous disease cytochrome b-negative  
autosomal recessive chronic granulomatous disease cytochrome b-positive type I  
autosomal recessive chronic granulomatous disease cytochrome b-positive type II  
autosomal recessive chronic granulomatous disease cytochrome b-positive type III  
autosomal recessive congenital ichthyosis +   
Autosomal Recessive Cutis Laxa +   
autosomal recessive distal spinal muscular atrophy 1  
autosomal recessive distal spinal muscular atrophy 2  
Autosomal Recessive Dyskeratosis Congenita +   
autosomal recessive early-onset Parkinson's disease 15  
autosomal recessive early-onset Parkinson's disease 23  
autosomal recessive early-onset Parkinson's disease 6  
autosomal recessive early-onset Parkinson's disease 7  
autosomal recessive Emery-Dreifuss muscular dystrophy 3  
autosomal recessive hypophosphatemic rickets +   
autosomal recessive isolated ectopia lentis 2  
autosomal recessive juvenile Parkinson's disease 2  
autosomal recessive limb-girdle muscular dystrophy +   
autosomal recessive non-syndromic intellectual disability +   
autosomal recessive nonsyndromic deafness +   
autosomal recessive osteopetrosis 1  
autosomal recessive osteopetrosis 2  
autosomal recessive osteopetrosis 3  
autosomal recessive osteopetrosis 4  
autosomal recessive osteopetrosis 5  
autosomal recessive osteopetrosis 6  
autosomal recessive osteopetrosis 7  
autosomal recessive osteopetrosis 8  
autosomal recessive Parkinson's disease 14  
autosomal recessive pericentral pigmentary retinopathy 
autosomal recessive polycystic kidney disease +   
autosomal recessive pseudohypoaldosteronism type 1  
autosomal recessive pyridoxine-refractory sideroblastic anemia 2  
autosomal recessive pyridoxine-refractory sideroblastic anemia 3  
autosomal recessive Robinow syndrome  
autosomal recessive type IV Ehlers-Danlos syndrome 
Bamforth-Lazarus syndrome  
Bardet-Biedl syndrome +   
Bart-Pumphrey syndrome  
Basaran Yilmaz Syndrome  
benign recurrent intrahepatic cholestasis 1  
benign recurrent intrahepatic cholestasis 2  
beta-ketothiolase deficiency  
Bird Headed Dwarfism Montreal Type 
Bjornstad syndrome  
Bloom syndrome  
Bowen-Conradi syndrome  
Brachycephaly, Trichomegaly, and Developmental Delay  
brachyolmia-amelogenesis imperfecta syndrome  
branched-chain keto acid dehydrogenase kinase deficiency  
camptodactyly-arthropathy-coxa vara-pericarditis syndrome  
Canavan disease  
Cardiac Conduction Disease with or without Dilated Cardiomyopathy  
cartilage-hair hypoplasia  
Catatrichy 
catecholaminergic polymorphic ventricular tachycardia 1  
CD3epsilon deficiency 
CD3gamma deficiency 
CD40 deficiency  
CEDNIK syndrome  
Charcot-Marie-Tooth disease recessive intermediate A  
Charcot-Marie-Tooth disease recessive intermediate B  
Charcot-Marie-Tooth disease recessive intermediate C  
Charcot-Marie-Tooth disease recessive intermediate D  
Chediak-Higashi syndrome +   
cleft lip-palate-ectodermal dysplasia syndrome  
Cockayne syndrome +   
cold-induced sweating syndrome +   
Cole Disease  
congenital disorder of glycosylation type IIa  
congenital disorder of glycosylation type IIb  
congenital disorder of glycosylation type IIc  
congenital disorder of glycosylation type IId  
congenital disorder of glycosylation type IIe  
congenital disorder of glycosylation type IIf  
congenital disorder of glycosylation type IIg  
congenital disorder of glycosylation type IIh  
congenital disorder of glycosylation type IIi  
congenital disorder of glycosylation type IIj  
congenital disorder of glycosylation type IIk  
congenital disorder of glycosylation type IIl  
congenital disorder of glycosylation type IIn  
congenital disorder of glycosylation type IIo  
congenital disorder of glycosylation type IIp  
congenital disorder of glycosylation type IIq  
Congenital Erythroderma with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-IgE  
Congenital Woolly Hair +   
Copper Deficiency, Familial Benign 
Corneodermatoosseous Syndrome 
craniolenticulosutural dysplasia  
Curly Hair-Ankyloblepharon-Nail Dysplasia Syndrome  
cystic fibrosis +   
Dermoodontodysplasia 
Diffuse Palmoplantar Keratoderma +   
dilated cardiomyopathy 1A  
dilated cardiomyopathy 1AA  
dilated cardiomyopathy 1B  
dilated cardiomyopathy 1BB  
dilated cardiomyopathy 1C  
dilated cardiomyopathy 1CC  
dilated cardiomyopathy 1D  
dilated cardiomyopathy 1DD  
dilated cardiomyopathy 1E  
dilated cardiomyopathy 1EE  
dilated cardiomyopathy 1FF  
dilated cardiomyopathy 1G  
dilated cardiomyopathy 1GG  
dilated cardiomyopathy 1H  
dilated cardiomyopathy 1HH  
dilated cardiomyopathy 1I  
dilated cardiomyopathy 1II  
dilated cardiomyopathy 1J  
dilated cardiomyopathy 1JJ  
dilated cardiomyopathy 1K 
dilated cardiomyopathy 1KK  
dilated cardiomyopathy 1L  
Dilated Cardiomyopathy 1LL  
dilated cardiomyopathy 1M  
dilated cardiomyopathy 1NN  
dilated cardiomyopathy 1O  
dilated cardiomyopathy 1P  
dilated cardiomyopathy 1Q 
dilated cardiomyopathy 1R  
dilated cardiomyopathy 1S  
dilated cardiomyopathy 1T  
dilated cardiomyopathy 1U  
dilated cardiomyopathy 1V  
dilated cardiomyopathy 1W  
dilated cardiomyopathy 1X  
dilated cardiomyopathy 1Y  
dilated cardiomyopathy 1Z  
dilated cardiomyopathy 2A  
dilated cardiomyopathy 2B  
dilated cardiomyopathy 2C  
Dilated Cardiomyopathy 3A  
Dilated Cardiomyopathy with Left Ventricular Noncompaction  
dilated cardiomyopathy with woolly hair and keratoderma +   
An autosomal recessive disease characterized by autosomal recessive inheritance of dilated cardiomyopathy, woolly hair, and keratoderma that has_material_basis_in homozygous mutation in the DSP gene on chromosome 6p24. (DO)
Dilated Cardiomyopathy, Right Ventricular 
Donnai-Barrow syndrome  
Donohue syndrome +   
Ectodermal Dysplasia 4, Hair/Nail Type  
Ectodermal Dysplasia 9, Hair/Nail Type  
Ehlers-Danlos syndrome progeroid type +   
Ellis-Van Creveld syndrome +   
epidermodysplasia verruciformis +   
epidermolysis bullosa simplex with muscular dystrophy  
familial erythrocytosis 2  
fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 1  
fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 2  
fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 3  
fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 4  
fibular hypoplasia and complex brachydactyly  
Fitzsimmons-McLachlan-Gilbert syndrome 
FLOTCH Syndrome 
folliculitis +   
Fraser syndrome +   
Galloway-Mowat syndrome +   
gangliosidosis +   
Griscelli syndrome +   
Hairy Palms and Soles 
hereditary spastic paraplegia 14 
hereditary spastic paraplegia 15  
hereditary spastic paraplegia 18  
hereditary spastic paraplegia 24 
hereditary spastic paraplegia 25 
hereditary spastic paraplegia 26  
hereditary spastic paraplegia 27 
hereditary spastic paraplegia 28  
hereditary spastic paraplegia 30  
hereditary spastic paraplegia 32 
hereditary spastic paraplegia 35  
hereditary spastic paraplegia 39  
hereditary spastic paraplegia 43  
hereditary spastic paraplegia 44  
hereditary spastic paraplegia 45  
hereditary spastic paraplegia 46  
hereditary spastic paraplegia 47  
hereditary spastic paraplegia 48  
hereditary spastic paraplegia 49  
hereditary spastic paraplegia 50  
hereditary spastic paraplegia 51  
hereditary spastic paraplegia 52  
hereditary spastic paraplegia 53  
hereditary spastic paraplegia 54  
hereditary spastic paraplegia 55  
hereditary spastic paraplegia 56  
hereditary spastic paraplegia 57  
hereditary spastic paraplegia 5A  
hereditary spastic paraplegia 61  
hereditary spastic paraplegia 63  
hereditary spastic paraplegia 64  
hereditary spastic paraplegia 7  
hereditary spastic paraplegia 74  
hereditary spastic paraplegia 75  
hereditary spastic paraplegia 76  
hereditary spastic paraplegia 77  
hereditary spastic paraplegia 9A  
hereditary spastic paraplegia 9B  
Hermansky-Pudlak syndrome +   
Hirsutism +   
hydrolethalus syndrome +   
Hyperkeratosis-Hyperpigmentation Syndrome 
hypertelorism, microtia, facial clefting syndrome 
hypertrichosis +   
hypertrophic cardiomyopathy 25  
hypomyelinating leukodystrophy 10  
hypomyelinating leukodystrophy 11  
hypomyelinating leukodystrophy 12  
hypomyelinating leukodystrophy 13  
hypomyelinating leukodystrophy 14  
hypomyelinating leukodystrophy 2  
hypomyelinating leukodystrophy 3  
hypomyelinating leukodystrophy 4  
hypomyelinating leukodystrophy 5  
hypomyelinating leukodystrophy 7 with or without oligodontia and-or hypogonadotropic hypogonadism  
hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism  
hypomyelinating leukodystrophy 9  
hypoparathyroidism-retardation-dysmorphism syndrome  
hypotrichosis +   
Hypotrichosis-Osteolysis-Periodontitis-Palmoplantar Keratoderma Syndrome 
immunodeficiency-centromeric instability-facial anomalies syndrome +   
JMP syndrome  
Johanson-Blizzard syndrome  
Judge Misch Wright Syndrome 
Kahrizi syndrome  
Kaler Garrity Stern Syndrome 
Katsantoni Papadakou Lagoyanni Syndrome 
Keratoderma Palmoplantaris Transgrediens 
Keratosis Focal Palmoplantar Gingival 
Keratosis Palmaris et Plantaris with Clinodactyly 
Keratosis Palmoplantaris Striata 1  
Keratosis Palmoplantaris Striata 2  
Keratosis Palmoplantaris Striata 3  
Keratosis Palmoplantaris with Esophageal Cancer  
Kozlowski-Krajewska Syndrome 
Krasnow Qazi Syndrome 
Laron syndrome +   
Laurence-Moon syndrome  
leukocyte adhesion deficiency +   
Leukoencephalomyelopathy  
mal de Meleda  
Malouf Syndrome  
Marinesco-Sjogren syndrome  
Martinez Monasterio Pinheiro Syndrome 
Meier-Gorlin syndrome +   
Menkes disease +   
microphthalmia with limb anomalies  
mitochondrial DNA depletion syndrome 1  
mitochondrial DNA depletion syndrome 11  
mitochondrial DNA depletion syndrome 12b  
mitochondrial DNA depletion syndrome 13  
mitochondrial DNA depletion syndrome 15  
mitochondrial DNA depletion syndrome 2  
mitochondrial DNA depletion syndrome 3  
mitochondrial DNA depletion syndrome 4A  
mitochondrial DNA depletion syndrome 4B  
mitochondrial DNA depletion syndrome 5  
mitochondrial DNA depletion syndrome 6  
mitochondrial DNA depletion syndrome 8A  
mitochondrial DNA depletion syndrome 9  
Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form, Autosomal Recessive +   
mitochondrial pyruvate carrier deficiency  
monilethrix +   
mulibrey nanism  
multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia and hydranencephaly  
multiple congenital anomalies-hypotonia-seizures syndrome 1  
multiple congenital anomalies-hypotonia-seizures syndrome 3  
multiple intestinal atresia  
multiple mitochondrial dysfunctions syndrome 1  
multiple mitochondrial dysfunctions syndrome 2  
multiple mitochondrial dysfunctions syndrome 3  
multiple mitochondrial dysfunctions syndrome 4  
multiple mitochondrial dysfunctions syndrome 5  
myofibrillar myopathy 1  
myofibrillar myopathy 7  
myofibrillar myopathy 8  
Naegeli Syndrome  
Nasu-Hakola disease  
Naxos Disease  
neonatal diabetes mellitus with congenital hypothyroidism  
nephronophthisis +   
nephrotic syndrome type 14  
nephrotic syndrome type 15  
nephrotic syndrome type 16  
Netherton syndrome  
Nijmegen breakage syndrome +   
nonepidermolytic palmoplantar keratoderma +   
nonphotosensitive trichothiodystrophy +   
oculocutaneous albinism +   
Oculotrichodysplasia 
orofaciodigital syndrome V  
osteoporosis-pseudoglioma syndrome  
ovarian dysgenesis 1  
ovarian dysgenesis 3  
ovarian dysgenesis 4  
ovarian dysgenesis 5  
ovarian dysgenesis 6  
ovarian dysgenesis 7  
Palmoplantar Hyperkeratosis and True Hermaphroditism  
Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and Sex Reversal  
PALMOPLANTAR KERATODERMA AND WOOLLY HAIR +   
Palmoplantar Keratoderma with Deafness  
Palmoplantar Keratoderma, Mutilating, with Periorificial Keratotic Plaques +   
Palmoplantar Keratoderma, Mutilating, with Periorificial Keratotic Plaques, X-Linked  
Palmoplantar Keratoderma, Nagashima Type  
Palmoplantar Keratoderma, Norrbotten Recessive Type 
Palmoplantar Keratoderma, Spastic Paralysis 
Papillon-Lefevre disease +   
Patel Bixler Syndrome 
Pedal Onychogryposis with Keratosis Plantaris and Coarse Hair 
Pendred syndrome  
peripartum cardiomyopathy  
PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT  
permanent neonatal diabetes mellitus +   
Perrault syndrome +   
PHARC syndrome  
Photosensitive Trichothiodystrophy 1  
Pierson syndrome  
Pili Annulati 
Pili Multigemini 
Pili Torti +  
POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY 2  
Porokeratosis 2, Palmar, Plantar, and Disseminated Type  
Powell Venencie Gordon syndrome 
progeria +   
prothrombin deficiency +   
pseudo-TORCH syndrome 1  
Pseudofolliculitis Barbae  
Pseudomonilethrix 
pseudoxanthoma elasticum +   
punctate palmoplantar keratoderma +   
rapadilino syndrome  
rhizomelic chondrodysplasia punctata +   
Riddle syndrome  
Roberts syndrome  
Rodrigues Blindness 
salt and pepper syndrome  
SC phocomelia syndrome  
Schopf-Schulz-Passarge Syndrome  
Schwartz-Jampel syndrome 1  
Seckel syndrome +   
Sengers syndrome  
Senior-Loken syndrome +   
Sensenbrenner syndrome +   
severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive  
sickle cell anemia +   
sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay  
Sjogren-Larsson syndrome +   
Skin Fragility-Woolly Hair Syndrome  
Sotos syndrome +   
spermatogenic failure 9  
spondyloepimetaphyseal dysplasia, Pakistani type  
spondyloepimetaphyseal dysplasia, Sponastrime type 
Stern Lubinsky Durrie Syndrome 
superficial mycosis +  
temtamy preaxial brachydactyly syndrome  
thalassemia +   
thiamine-responsive megaloblastic anemia syndrome  
tinea capitis +  
Tricho-Dento-Osseous Syndrome  
Tricho-Dento-Osseous Syndrome 1 
Trichodysplasia-Xeroderma 
Trichohepatoenteric Syndrome  
Trichohepatoenteric Syndrome 2  
TRICHOMEGALY  
trichorhinophalangeal syndrome type I  
trichorhinophalangeal syndrome type III  
Trichostasis Spinulosa 
trimethylaminuria  
triple-A syndrome  
Uhl Anomaly 
Uncombable Hair Syndrome +   
urofacial syndrome +   
Usher syndrome +   
UV-sensitive syndrome +   
Vici syndrome  
Vohwinkel Syndrome  
Warburg micro syndrome +   
Werner syndrome +   
White Forelock with Malformations 
Winship Viljoen Leary Syndrome 
Wolcott-Rallison syndrome  
Woolly Hair, Autosomal Recessive +   
X-linked dilated cardiomyopathy  
xeroderma pigmentosum +   

Synonyms
Exact Synonyms: Carvajal syndrome ;   DCWHK ;   Epidermolytic palmoplantar keratoderma, woolly hair, and dilated cardiomyopathy ;   dilated cardiomyopathy, woolly hair, keratoderma ;   palmoplantar keratoderma with left ventricular cardiomyopathy and woolly hair
Primary IDs: MESH:C535581
Alternate IDs: OMIM:605676 ;   RDO:0000792

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