Ontology Browser

Term:
Glomerulonephritis with Sparse Hair and Telangiectases (DOID:9006306)
Annotations: Rat: (2) Mouse: (2) Human: (2) Chinchilla: (2) Bonobo: (1) Dog: (2) Squirrel: (2)
Parent Terms Term With Siblings Child Terms
alopecia areata +   
Alopecia Congenita Keratosis Palmoplantaris +   
Alopecia Contractures Dwarfism Mental Retardation 
Alopecia Epilepsy Oligophrenia Syndrome of Moynahan 
alopecia universalis +   
Alopecia Universalis Congenita, XY Gonadal Dysgenesis, and Laryngomalacia 
Alopecia, Epilepsy, Pyorrhea, Mental Subnormality 
Alopecia, Hypogonadism, Extrapyramidal Disorder 
Alopecia, Neurologic Defects, and Endocrinopathy Syndrome  
Alopecia-Mental Retardation Syndrome +   
Androgenetic Alopecia 2 
Androgenetic Alopecia 3 
androgenic alopecia 
atrichia with papular lesions  
Bullous Dystrophy, Hereditary Macular Type 
Cancer, Alopecia, Pigment Dyscrasia, Onychodystrophy, and Keratoderma  
Cataract, Alopecia, Sclerodactyly 
Central Centrifugal Cicatricial Alopecia  
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy  
CFHR5 Deficiency  
Congenital Alopecia X-Linked 
Cutaneous Telangiectasia and Cancer Syndrome, Familial  
Dermatopathia Pigmentosa Reticularis  
Ectodermal Dysplasia Alopecia Preaxial Polydactyly 
Ectodermal Dysplasia Syndrome with Distinctive Facial Appearance and Preaxial Polydactyly of Feet 
Familial Focal Alopecia 
Follicular Hamartoma, Alopecia, Cystic Fibrosis 
follicular mucinosis 
Frontonasal Dysplasia 2  
Garret Tripp Syndrome 
Glomerulonephritis with Isolated C3 Deposits and Factor H Deficiency  
Glomerulonephritis with Isolated C3 Deposits and Factor I Deficiency 
Glomerulonephritis with Sparse Hair and Telangiectases  
Glomerulopathy with Giant Fibrillar Deposits  
Gomez Lopez Hernandez Syndrome 
Growth Retardation, Alopecia, Pseudoanodontia and Optic Atrophy  
Hypergonadotropic Hypogonadism And Partial Alopecia 
hypotrichosis 7  
Ichthyosis Follicularis Atrichia Photophobia Syndrome  
Jagell Holmgren Hofer Syndrome 
Johnson Neuroectodermal Syndrome 
Keratosis Follicularis Spinulosa Decalvans, Autosomal Dominant 
Kuster Majewski Hammerstein Syndrome 
Loose Anagen Hair Syndrome +   
Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis  
mandibulofacial dysostosis with alopecia  
Membranoproliferative Glomerulonephritis, X-Linked 
Microcephaly Sparse Hair Mental Retardation Seizures 
Moloney Syndrome 
MPGN II with Complement Factor H Deficiency 
nephrotic syndrome type 7  
Nisch syndrome  
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 

Synonyms
Exact Synonyms: Cutaneous telangiectasia, sparse hair and membranoproliferative glomerulonephritis ;   HLTRS ;   HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME ;   Telangiectatic membranoproliferative glomerulonephritis ;   glomerulonephritis, sparse hair, telangiectases
Primary IDs: MESH:C536825
Alternate IDs: OMIM:137940 ;   RDO:0002518 ;   RDO:0016131

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.