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Ontology Browser
Term:
HYPERTELORISM, PREAURICULAR SINUS, PUNCTAL PITS, AND DEAFNESS (DOID:9001647)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0)
Parent Terms Term With Siblings Child Terms
auditory system disease +     
Deafness +     
Hypertelorism +     
lacrimal duct obstruction +     
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome  
Absence of Tibia with Congenital Deafness 
Acrootoocular Syndrome 
ADULT syndrome  
Albinism Deafness Syndrome 
Arthrogryposis Multiplex with Deafness, Inguinal Hernias, and Early Death 
Atrial Septal Defect, Secundum, with Various Cardiac and Noncardiac Defects 
auditory system benign neoplasm +  
Auriculocondylar Syndrome +   
autosomal dominant congenital deafness with onychodystrophy  
autosomal dominant nonsyndromic deafness 65  
Ayazi Syndrome 
Bagatelle Cassidy syndrome 
Barber-Say syndrome  
Branchiogenic-Deafness Syndrome 
Burn-McKeown syndrome  
Camptodactyly Syndrome Guadalajara Type 2 
Camptodactyly Syndrome Guadalajara Type 3 
Cardioauditory Syndrome of Sanchez Cascos 
Chitty Hall Baraitser Syndrome 
chromosome 6pter-p24 deletion syndrome 
COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS  
Congenital Deafness and Familial Myoclonic Epilepsy 
Congenital Deafness, with Vitiligo and Achalasia 
Congenital Emphysema, with Deafness, Penoscrotal Web, and Mental Retardation 
Congenital Microtia +   
Congenital Myopathy with Neuropathy and Deafness  
Coxoauricular Syndrome 
Davenport Donlan Syndrome 
De Hauwere Leroy Adriaenssens syndrome 
De Hauwere 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  
Dislocated Elbows, Bowed Tibias, Scoliosis, Deafness, Cataract, Microcephaly, and Mental Retardation 
Ear Deformities, Acquired 
Ear Neoplasms +  
Earache 
Epiphyseal Dysplasia of Femoral Head, Myopia, and Deafness 
external ear disease +   
Facial Abnormalities, Kyphoscoliosis, and Mental Retardation 
Fine-Lubinsky Syndrome 
Fountain Syndrome 
frontonasal dysplasia 1  
frontonasal dysplasia 2  
frontonasal dysplasia 3  
Gastrocutaneous Syndrome 
Gillessen-Kaesbach-Nishimura Dysplasia  
Hamamy Syndrome  
Hearing Disorders +   
hereditary spastic paraplegia 24 
herpes zoster oticus 
Herrmann Syndrome 
high myopia-sensorineural deafness syndrome  
Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness 
Hyperlipoproteinemia Type II, and Deafness 
Hyperphosphatasia with Mental Retardation Syndrome 1  
Hypertelorism and Tetralogy of Fallot  
HYPERTELORISM, PREAURICULAR SINUS, PUNCTAL PITS, AND DEAFNESS 
Hypokalemic Tubulopathy and Deafness  
Hypospadias, Hypertelorism, Upper Lid Coloboma, and Mixed-Type Hearing Loss 
inner ear disease +   
INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPERTELORISM AND DISTINCTIVE FACIES  
ITM2B-related cerebral amyloid angiopathy 2  
Johnson Neuroectodermal Syndrome 
Jones Syndrome 
Keipert syndrome  
Keratitis-Ichthyosis-Deafness Syndrome +   
Konigsmark Knox Hussels Syndrome 
Krauss Herman Holmes Syndrome 
Lachiewicz Sibley Syndrome 
Lacrimal Puncta Agenesis  
LEUKOENCEPHALOPATHY, PROGRESSIVE, INFANTILE-ONSET, WITH OR WITHOUT DEAFNESS  
Lynch Lee Murday syndrome 
Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome  
Marles Greenberg Persaud Syndrome  
Meyenburg-Altherr-Uehlinger Syndrome 
Microcephaly Deafness Syndrome 
middle ear disease +   
Muckle-Wells syndrome  
Multiple Synostoses Syndrome 1  
Myoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders 
Myoclonus, Cerebellar Ataxia, and Deafness 
Naguib-Richieri-Costa Syndrome 
Nathalie Syndrome 
necrosis of ear ossicle 
Nephrosis Deafness Urinary Tract Digital Malformation 
Neuromuscular Oculoauditory Syndrome  
Noninsulin-Dependent Diabetes Mellitus with Deafness  
nonsyndromic deafness +   
Opitz-GBBB syndrome +   
Opticocochleodentate Degeneration 
Otitis +   
otorrhea 
Perrault syndrome +   
Preauricular Tag, Isolated, Autosomal Dominant, 1  
Primrose Syndrome  
Question Mark Ears, Isolated  
Ramos Arroyo Clark Syndrome 
retrocochlear disease +   
Ribbonlike Corneal Degeneration with Deafness 
Richards-Rundle Syndrome 
Roberts syndrome  
Santos Mateus Leal Syndrome 
Schimke X-Linked Mental Retardation Syndrome 
Schlegelberger Grote Syndrome 
Schwartz-Lelek Syndrome  
Seaver Cassidy Syndrome 
Secretory Diarrhea, Myopathy, and Deafness 
SIDDIQI SYNDROME  
Sinoatrial Node Dysfunction and Deafness  
Supernumerary Der(22)t(8 
Susac Syndrome 
syndactyly-telecanthus-anogenital and renal malformations syndrome  
tarsal-carpal coalition syndrome +   
Teebi Hypertelorism Syndrome +   
temtamy preaxial brachydactyly syndrome  
Tietz syndrome  
Tympanic Membrane Perforation  
tympanosclerosis  
Wells Jankovic Syndrome 
Wright Dyck 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 

Synonyms
Exact Synonyms: HPPD
Primary IDs: OMIM:614187 ;   RDO:0010100

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