Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
alopecia +     
Anosmia +     
Deafness +     
hypogonadism +     
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome  
Absence of Tibia with Congenital Deafness 
Albinism Deafness Syndrome 
alopecia areata +   
Alopecia Congenita Keratosis Palmoplantaris +   
Alopecia Contractures Dwarfism Mental Retardation 
alopecia universalis +   
Alopecia, Epilepsy, Pyorrhea, Mental Subnormality 
Alopecia, Hypogonadism, Extrapyramidal Disorder  
alopecia, neurologic defects, and endocrinopathy syndrome  
Alopecia-Epilepsy-Oligophrenia Syndrome of Moynahan 
alopecia-mental retardation syndrome +   
Alopecia-Mental Retardation Syndrome with Convulsions and Hypergonadotropic Hypogonadism 
Androgenetic Alopecia 2 
Androgenetic Alopecia 3 
androgenic alopecia  
Arthrogryposis Multiplex with Deafness, Inguinal Hernias, and Early Death 
ataxia telangiectasia +   
atrichia with papular lesions  
autosomal dominant congenital deafness with onychodystrophy  
autosomal dominant keratosis follicularis spinulosa decalvans 
autosomal dominant nonsyndromic deafness 65  
Ayazi Syndrome 
Bassoe Syndrome 
Biemond Syndrome II 
Borjeson-Forssman-Lehmann syndrome  
Boucher-Neuhauser syndrome  
Branchiogenic-Deafness Syndrome 
Bullous Dystrophy, Hereditary Macular Type 
Burn-McKeown syndrome  
Cancer, Alopecia, Pigment Dyscrasia, Onychodystrophy, and Keratoderma  
Cantalamessa Baldini Ambrosi Syndrome 
Cardioauditory Syndrome of Sanchez Cascos 
Cardiomyopathy Hypogonadism Collagenoma Syndrome 
CEDNIK syndrome  
Central Centrifugal Cicatricial Alopecia  
Cerebellar Ataxia and Hypergonadotropic Hypogonadism 
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy  
Chang Davidson Carlson Syndrome 
chemotherapy-induced alopecia  
CHIME syndrome  
Chudley-Rozdilsky Syndrome 
COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS  
Congenital Alopecia X-Linked 
Congenital Anosmia +   
Congenital Deafness and Familial Myoclonic Epilepsy 
Congenital Deafness, with Vitiligo and Achalasia 
Congenital Emphysema, with Deafness, Penoscrotal Web, and Mental Retardation 
Congenital Infantile Muscular Dystrophy with Cataract and Hypogonadism 
Congenital Myopathy with Neuropathy and Deafness  
Coxoauricular Syndrome 
Cutaneous Telangiectasia and Cancer Syndrome, Familial  
Davenport Donlan Syndrome 
De Sanctis-Cacchione syndrome  
Deaf-Blind Disorders +   
Deafness Hyperuricemia Neurologic Ataxia 
Deafness with Anhidrotic Ectodermal Dysplasia 
Deafness, Autosomal Dominant, due to Mutation In Myo1a 
DEAFNESS, CATARACT, IMPAIRED INTELLECTUAL DEVELOPMENT, AND POLYNEUROPATHY  
Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities 
Deafness, Congenital Onychodystrophy, Recessive Form 
DEAFNESS, CONGENITAL, AND ADULT-ONSET PROGRESSIVE LEUKOENCEPHALOPATHY  
Deafness, with Smith-Magenis Syndrome  
Deafness-Hypogonadism Syndrome 
dermatopathia pigmentosa reticularis  
Dislocated Elbows, Bowed Tibias, Scoliosis, Deafness, Cataract, Microcephaly, and Mental Retardation 
Ectodermal Dysplasia Syndrome with Distinctive Facial Appearance and Preaxial Polydactyly of Feet 
Ectodermal Dysplasia, Alopecia, Preaxial Polydactyly 
Elejalde Disease 
Encephalocraniocutaneous Lipomatosis  
Encephalopathy, Spastic Tetraparesis, and Hypogonadism 
Epiphyseal Dysplasia of Femoral Head, Myopia, and Deafness 
eunuchism +   
Familial Focal Alopecia 
Fine-Lubinsky Syndrome  
Follicular Hamartoma, Alopecia, Cystic Fibrosis 
follicular mucinosis 
Fountain Syndrome 
frontal fibrosing alopecia  
frontonasal dysplasia 2  
GAPO syndrome  
Garret Tripp Syndrome 
Gomez Lopez Hernandez Syndrome 
gonadal dysgenesis +   
GROWTH RESTRICTION, HYPOPLASTIC KIDNEYS, ALOPECIA, AND DISTINCTIVE FACIES  
Hereditary Neurocutaneous Angioma 
Hereditary Sensory and Autonomic Neuropathy, Adult-Onset, with Anosmia 
hereditary spastic paraplegia 24 
Herrmann Syndrome 
high myopia-sensorineural deafness syndrome  
Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness 
Hypergonadotropic Hypogonadism and Partial Alopecia 
Hyperlipoproteinemia Type II, and Deafness 
HYPERTELORISM, PREAURICULAR SINUS, PUNCTAL PITS, AND DEAFNESS 
Hypogonadism and Testicular Atrophy  
Hypogonadism with Low-Grade Mental Deficiency and Microcephaly 
hypogonadotropic hypogonadism +   
Hypokalemic Tubulopathy and Deafness  
hypomyelinating leukodystrophy 7  
hypotrichosis 7  
hypotrichosis-lymphedema-telangiectasia-renal defect syndrome  
Ichthyosis and Male Hypogonadism 
ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis  
IFAP Syndrome +   
Isolated Mineralocorticoid Deficiency  
ITM2B-related cerebral amyloid angiopathy 2  
Jagell Holmgren Hofer Syndrome 
Johnson Neuroectodermal Syndrome 
Jones Syndrome 
Keipert syndrome  
Keratitis-Ichthyosis-Deafness Syndrome +   
Klinefelter syndrome  
Konigsmark Knox Hussels Syndrome 
Kuster Majewski Hammerstein Syndrome 
LEUKOENCEPHALOPATHY, PROGRESSIVE, INFANTILE-ONSET, WITH OR WITHOUT DEAFNESS  
linear nevus sebaceous syndrome +   
loose anagen hair syndrome +   
Lubinsky Syndrome 
Lynch Lee Murday syndrome 
Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis  
Male Hypogonadism with Mental Retardation and Skeletal Anomalies 
Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome  
mandibulofacial dysostosis with alopecia  
Martsolf Syndrome +   
MEHMO syndrome  
Meyenburg-Altherr-Uehlinger Syndrome 
Microcephaly Deafness Syndrome 
Microcephaly Sparse Hair Mental Retardation Seizures 
Moebius Axonal Neuropathy Hypogonadism 
Moloney Syndrome 
Moyamoya Disease 4 with Short Stature, Hypergonadotropic Hypogonadism, and Facial Dysmorphism 
Muckle-Wells syndrome  
multiple synostoses syndrome 1  
Myoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders 
Myoclonus, Cerebellar Ataxia, and Deafness 
Myopathy, Cataract, Hypogonadism Syndrome 
Nathalie Syndrome 
Nephrosis with Deafness and Urinary Tract and Digital Malformations 
Neurocutaneous Melanosis  
Neurodevelopmental Disorder with Alopecia and Brain Abnormalities  
neurofibromatosis +   
Noninsulin-Dependent Diabetes Mellitus with Deafness  
nonsyndromic deafness +   
Opticocochleodentate Degeneration 
palmoplantar keratoderma and congenital alopecia 2 
PARC Syndrome 
Patel Bixler Syndrome 
Perniola Krajewska Carnevale Syndrome 
Perrault syndrome +   
PHACE Association  
Phacomatosis Pigmentovascularis 
Progressive External Ophthalmoplegia with Hypogonadism 
Ramos Arroyo Clark Syndrome 
Retinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism 
Ribbonlike Corneal Degeneration with Deafness 
Richards-Rundle Syndrome 
Rud Syndrome 
Satoyoshi Syndrome 
Schimke X-Linked Mental Retardation Syndrome 
Schlegelberger Grote Syndrome 
Scholte Syndrome 
Secretory Diarrhea, Myopathy, and Deafness 
Seemanova Lesny Syndrome 
Sexual Infantilism  
Siddiqi syndrome  
Sinoatrial Node Dysfunction and Deafness  
Slti Salem Syndrome 
spastic paraplegia with deafness 
Sturge-Weber syndrome +   
syndromic X-linked intellectual disability Cabezas type  
T-cell immunodeficiency, congenital alopecia, and nail dystrophy  
telogen effluvium 
temtamy preaxial brachydactyly syndrome  
Thumb Deformity and Alopecia 
Thumb Deformity, Alopecia, Pigmentation Anomaly 
Tietz syndrome  
tuberous sclerosis +   
Urban Schosser Spohn Syndrome  
Vasquez Hurst Sotos Syndrome 
von Hippel-Lindau disease  
Warburg micro syndrome +   
Weinstein Kliman Scully Syndrome 
Woodhouse-Sakati syndrome  
Woolly Hair, Hypotrichosis, Everted Lower Lip and Outstanding Ears 
Wright Dyck Syndrome 
Wyburn Mason's Syndrome 
X-linked Alport syndrome  
X-linked mental retardation Gustavson type  
X-linked mental retardation-hypotonic facies syndrome-1  
X-linked retinitis pigmentosa and sinorespiratory infections  
Yemenite Deaf-Blind Hypopigmentation Syndrome 
Young Hughes Syndrome 

Synonyms
Exact Synonyms: AADH syndrome ;   Alopecia anosmia deafness hypogonadism syndrome ;   Johnson-Mcmillin syndrome
Primary IDs: MESH:C535882
Alternate IDs: MIM:147770

paths to the root