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Term:
Multiple Noduli Cutanei with Urinary Tract Abnormalities (DOID:9003396)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0)
Parent Terms Term With Siblings Child Terms
hydronephrosis +     
Absence of Fingerprints  
Actinic Prurigo  
Agenesis of Corpus Callosum with Facial Anomalies and Robin Sequence 
Albinism +   
Allanson Pantzar McLeod Syndrome +   
Alport syndrome +   
Annular Erythema 
Antley-Bixler Syndrome with Genital Anomalies and Disordered Steroidogenesis  
arterial tortuosity syndrome  
atopic dermatitis +   
Atrioventricular Septal Defect with Blepharophimosis and Anal and Radial Defects 
Atrophia Maculosa Varioliformis Cutis, Familial 
AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS  
autosomal recessive congenital ichthyosis +   
B-Cell Immunodeficiency, Distal Limb Anomalies, and Urogenital Malformations 
Basaloid Follicular Hamartoma Syndrome, Generalized, Autosomal Dominant 
Beaulieu-Boycott-Innes Syndrome  
Bifid or Double Ureter 
blepharophimosis, ptosis, and epicanthus inversus syndrome  
Bloch-Sulzberger syndrome +   
bullous congenital ichthyosiform erythroderma  
Buschke-Ollendorff Syndrome  
CAKUT2  
Calabro Syndrome 
chromosome 1p32-p31 deletion syndrome  
Cleft Palate, Cardiac Defect, Genital Anomalies, and Ectrodactyly 
Collagenosis, Familial Reactive Perforating 
Congenital Erythroderma with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-IgE  
Congenital Hydronephrosis, with Cleft Palate, Characteristic Facies, Hypotonia, and Mental Retardation 
cryptorchidism +   
Cutaneous Bullous Amyloidosis 
cutaneous porphyria  
cutis laxa +   
DK Phocomelia Syndrome 
Dowling-Degos disease +   
Duker Weiss Siber syndrome 
dyschromatosis universalis hereditaria +   
dyskeratosis congenita +   
ectodermal dysplasia +   
Ehlers-Danlos syndrome +   
epidermolysis bullosa +   
Epispadias +   
erythrokeratodermia variabilis +   
Erythrokeratodermia with Ataxia  
Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa of Siemens-like  
Follicular Atrophoderma, Perioral Pigmented, with Milia and Epidermoid Cysts 
Fraser syndrome +   
Fused Kidney  
Genitopatellar Syndrome  
Genitourinary Tract Anomalies 
Gerodermia Osteodysplastica  
Hailey-Hailey disease  
hand-foot-genital syndrome  
Hepatic Porphyrias +   
Hereditary Autoinflammatory Diseases +   
hereditary mucosal leukokeratosis  
Histiocytic Dermatoarthritis 
Hyaluronan Metabolism, Defect in 
hypospadias +   
ichthyosis vulgaris +   
IMAGe syndrome  
IMAGEI Syndrome  
Isolated Osteopoikilosis 
Juvenile Spring Eruption of Ears 
Keratolytic Winter Erythema  
keratosis follicularis +   
Keratosis Follicularis Spinulosa Decalvans, X-Linked  
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma  
Lethal Congenital Nonspherocytic Hemolytic Anemia with Genital and Other Abnormalities 
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis 
lipoid proteinosis  
Lissencephaly, X-Linked, 2  
Microcephaly Seizures Genital Hypoplasia 
Microphthalmia, Syndromic 6  
monilethrix +   
Muir-Torre syndrome  
Multicystic Dysplastic Kidney +   
Multiple Noduli Cutanei with Urinary Tract Abnormalities 
Myotubular Myopathy with Abnormal Genital Development 
Nephrosis Deafness Urinary Tract Digital Malformation 
Oculotrichodysplasia 
Omphalocele Exstrophy Imperforate Anus 
orofaciodigital syndrome IX  
palmoplantar keratosis +   
Parana Hard Skin Syndrome 
Pedal Onychogryposis with Keratosis Plantaris and Coarse Hair 
peeling skin syndrome +   
Perifolliculitis Capitis Abscedens Et Suffodiens, Familial 
Piepkorn Karp Hickok syndrome 
Plasminogen Deficiency, Type I  
Poikiloderma, Hereditary Sclerosing +   
popliteal pterygium syndrome +   
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  
Proud Syndrome  
pseudoxanthoma elasticum +   
Pyelectasis 
Pyonephrosis 
renal agenesis +   
Renal Dysplasia - Limb Defects Syndrome 
Renal, Genital, and Middle Ear Anomalies 
Reticulate Pigmentary Disorder, with Systemic Manifestations  
Retrocaval Ureter 
Robinow syndrome +   
Rosselli-Gulienetti Syndrome 
Rothmund-Thomson syndrome +   
sex development disorder +   
Sjogren-Larsson syndrome +   
Skin Fragility-Woolly Hair Syndrome  
Split-Hand with Obstructive Uropathy, Spina Bifida, and Diaphragmatic Defects 
Spondylocostal Dysostosis with Anal Atresia and Urogenital Anomalies 
Stiff Skin Syndrome  
Storm Syndrome 
Structural Heart Defects and Renal Anomalies Syndrome  
Systemic Hyalinosis  
Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations  
Trichothiodystrophy Syndromes +   
Urethral Obstruction Sequence 
Urinary Fistula +  
Uterine Anomalies 
Vohwinkel Syndrome, Variant Form  
X-linked ichthyosis +   
xeroderma pigmentosum +   

Synonyms
Primary IDs: MESH:C563512
Alternate IDs: RDO:0012750

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