Ontology Browser

Term:
Oculotrichodysplasia (DOID:9004081)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0)
Parent Terms Term With Siblings Child Terms
hair disease +     
Malformed Nails +     
Absence of Fingerprints  
Ackerman Syndrome 
Actinic Prurigo  
ADULT syndrome  
Albinism +   
Aldred Syndrome 
Alopecia Universalis, Onychodystrophy, Vitiligo 
Alstrom syndrome  
Amaurosis Hypertrichosis  
Ameloonychohypohidrotic Syndrome 
Annular Erythema 
anodontia +   
anonychia congenita +   
Anonychia Onychodystrophy 
Anonychia with Flexural Pigmentation 
Anonychia-Ectrodactyly 
Anterior Segment Dysgenesis 4  
AREDYLD Syndrome 
arterial tortuosity syndrome  
atopic dermatitis +   
Atrophia Maculosa Varioliformis Cutis, Familial 
AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS  
autosomal recessive congenital ichthyosis +   
autosomal recessive pericentral pigmentary retinopathy 
Bamforth-Lazarus syndrome  
Basaloid Follicular Hamartoma Syndrome, Generalized, Autosomal Dominant 
Basan Syndrome  
Bird Headed Dwarfism Montreal Type 
Bjornstad syndrome  
blepharocheilodontic syndrome +   
Bloch-Sulzberger syndrome +   
Book Syndrome 
Bork Stender Schmidt Syndrome 
Brachycephaly, Trichomegaly, and Developmental Delay  
Brachymorphism-Onychodysplasia-Dysphalangism Syndrome 
bullous congenital ichthyosiform erythroderma  
Buschke-Ollendorff Syndrome  
Cancer, Alopecia, Pigment Dyscrasia, Onychodystrophy, and Keratoderma 
Carabelli Anomaly of Maxillary Molar Teeth 
Cartwright Nelson Fryns Syndrome 
Catatrichy 
Chang Davidson Carlson Syndrome 
Chromosome Xp11.3 Deletion Syndrome  
Cleidocranial Dysplasia, Forme Fruste, Dental Anomalies Only  
CODAS Syndrome  
Collagenosis, Familial Reactive Perforating 
Cone Dystrophy 4  
Cone Dystrophy, X-Linked, with Tapetal-like Sheen 
Cone Rod Dystrophy Amelogenesis Imperfecta  
cone-rod dystrophy 1  
cone-rod dystrophy 10  
cone-rod dystrophy 11  
cone-rod dystrophy 12  
cone-rod dystrophy 13  
cone-rod dystrophy 14  
cone-rod dystrophy 16  
cone-rod dystrophy 17 
cone-rod dystrophy 18  
cone-rod dystrophy 19  
cone-rod dystrophy 2  
cone-rod dystrophy 20  
Cone-Rod Dystrophy 21  
cone-rod dystrophy 3  
cone-rod dystrophy 5  
cone-rod dystrophy 6  
cone-rod dystrophy 7  
cone-rod dystrophy 8 
Congenital Deafness with Inner Ear Agenesis, Microtia, and Microdontia  
Congenital Deafness, and Onychodystrophy, Autosomal Dominant  
Congenital Erythroderma with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-IgE  
Congenital Woolly Hair +   
Copper Deficiency, Familial Benign 
Craniosynostosis and Dental Anomalies  
Curly Hair-Acral Keratoderma-Caries Syndrome 
Curly Hair-Ankyloblepharon-Nail Dysplasia Syndrome  
Cutaneous Bullous Amyloidosis 
cutaneous porphyria  
cutis laxa +   
Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness  
Deafness Enamel Hypoplasia Nail Defects  
Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities 
Dens in Dente +  
dental enamel hypoplasia +   
dentin dysplasia +   
dentinogenesis imperfecta +   
Dermoodontodysplasia 
Diastema +  
Digitorenocerebral Syndrome  
dilated cardiomyopathy with woolly hair and keratoderma +   
Dilated Cardiomyopathy with Woolly Hair, Keratoderma, and Tooth Agenesis  
dominant pericentral pigmentary retinopathy 
Double Nail for Fifth Toe 
Dowling-Degos disease +   
dyschromatosis universalis hereditaria +   
dyskeratosis congenita +   
ectodermal dysplasia +   
Ectodermal Dysplasia 4, Hair/Nail Type  
Ectodermal Dysplasia 9, Hair/Nail Type  
Ehlers-Danlos syndrome +   
epidermolysis bullosa +   
epidermolytic hyperkeratosis +   
erythrokeratodermia variabilis +   
Erythrokeratodermia with Ataxia  
Euhidrotic Ectodermal Dysplasia 
Faciocardiomelic Dysplasia, Lethal 
FLOTCH Syndrome 
Flynn Aird Syndrome 
folliculitis +   
Furukawa Takagi Nakao Syndrome 
Fused Teeth 
Gerodermia Osteodysplastica  
Gorlin Bushkell Jensen Syndrome 
Grubben de Cock Borghgraef Syndrome 
Hailey-Hailey disease  
Hairy Palms and Soles 
Hardikar Syndrome 
Hepatic Porphyrias +   
Hereditary Autoinflammatory Diseases +   
Hereditary Koilonychia 
hereditary mucosal leukokeratosis  
Hereditary Sclerosing Poikiloderma +   
Hirsutism +   
Histiocytic Dermatoarthritis 
Hyaluronan Metabolism, Defect in 
hypertrichosis +   
Hypoglossia-Hypodactylia 
Hypospadias-Mental Retardation Syndrome 
HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME  
hypotrichosis +   
ichthyosis vulgaris +   
isolated microphthalmia 5  
Isolated Osteopoikilosis 
Jalili Syndrome  
Juvenile Spring Eruption of Ears 
Kaler Garrity Stern Syndrome 
Katsantoni Papadakou Lagoyanni Syndrome 
KBG syndrome  
Kearns-Sayre syndrome  
Keratolytic Winter Erythema  
keratosis follicularis +   
Keratosis Follicularis Spinulosa Decalvans, X-Linked  
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma  
Kozlowski-Krajewska Syndrome 
Kumar Levick Syndrome 
LADD syndrome  
Larsen syndrome  
late-adult onset retinitis pigmentosa 
Leber congenital amaurosis 14  
Leber congenital amaurosis 3  
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis 
Light Fixation Seizure Syndrome 
lipoid proteinosis  
MACULAR DYSTROPHY WITH CENTRAL CONE INVOLVEMENT  
Mammary-Digital-Nail Syndrome 
Martinez Monasterio Pinheiro Syndrome 
Menkes disease +   
Metaphyseal Chondrodysplasia with Retinitis Pigmentosa  
Microcephaly, Retinitis Pigmentosa, and Sutural Cataract 
Mirhosseini-Holmes-Walton Syndrome 
monilethrix +   
Muir-Torre syndrome  
Multiple Noduli Cutanei with Urinary Tract Abnormalities 
Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus 
Nance-Horan syndrome  
Naxos Disease  
Neuropathy Ataxia and Retinitis Pigmentosa  
Newfoundland cone-rod dystrophy  
nonsyndromic congenital nail disorder 1 
nonsyndromic congenital nail disorder 10  
nonsyndromic congenital nail disorder 8  
nonsyndromic congenital nail disorder 9  
oculodentodigital dysplasia +   
Oculotrichodysplasia 
Odontodysplasia +   
Odontomicronychial Dysplasia 
Odontotrichoungual-Digital-Palmar Syndrome 
Oliver-McFarlane Syndrome  
Onycholysis, Partial, with Scleronychia 
Onychotrichodysplasia and Neutropenia 
Oroacral Syndrome, Verloes-Koulischer Type 
orofaciodigital syndrome IX  
Otodental Dysplasia 
Otoonychoperoneal Syndrome 
Pallidal Degeneration, Progressive, with Retinitis Pigmentosa 
palmoplantar keratosis +   
Parana Hard Skin Syndrome 
Pedal Onychogryposis with Keratosis Plantaris and Coarse Hair 
peeling skin syndrome +   
Perifolliculitis Capitis Abscedens Et Suffodiens, Familial 
Perioral Pigmented Follicular Atrophoderma with Milia and Epidermoid Cysts 
Peripheral Cone Dystrophy 
PHARC syndrome  
Photosensitive Trichothiodystrophy 1  
Pigmentary Retinopathy and Sensorineural Deafness  
Pili Annulati 
Pili Multigemini 
Pili Torti +  
Pili Torti Onychodysplasia 
Pinheiro Freire-Maia Miranda Syndrome 
Plasminogen Deficiency, Type I  
porokeratosis +   
Postaxial Polydactyly, with Dental and Vertebral Anomalies 
Posterior Column Ataxia with Retinitis Pigmentosa  
primary cutaneous amyloidosis +   
Progressive Osseous Heteroplasia  
Progressive Vitiligo with Mental Retardation and Urethral Duplication 
Prolidase Deficiency  
Pseudofolliculitis Barbae  
Pseudomonilethrix 
pseudoxanthoma elasticum +   
Radioulnar Synostosis Retinal Pigment Abnormalities 
Reticulate Pigmentary Disorder, with Systemic Manifestations  
Retinal Cone Dystrophy 3A  
Retinal Cone Dystrophy 3B  
Retinal Cone Dystrophy 4  
retinitis pigmentosa 1  
retinitis pigmentosa 10  
retinitis pigmentosa 11  
retinitis pigmentosa 12  
retinitis pigmentosa 13  
retinitis pigmentosa 14  
retinitis pigmentosa 17  
retinitis pigmentosa 18  
retinitis pigmentosa 19  
retinitis pigmentosa 2  
retinitis pigmentosa 20  
retinitis pigmentosa 22 
retinitis pigmentosa 23  
retinitis pigmentosa 24 
retinitis pigmentosa 25  
retinitis pigmentosa 26  
retinitis pigmentosa 27  
retinitis pigmentosa 28  
retinitis pigmentosa 29 
retinitis pigmentosa 3  
retinitis pigmentosa 30  
retinitis pigmentosa 31  
retinitis pigmentosa 32 
retinitis pigmentosa 33  
retinitis pigmentosa 34 
retinitis pigmentosa 35  
retinitis pigmentosa 36  
retinitis pigmentosa 37  
retinitis pigmentosa 38  
retinitis pigmentosa 39  
retinitis pigmentosa 4  
retinitis pigmentosa 40  
retinitis pigmentosa 41  
retinitis pigmentosa 42  
retinitis pigmentosa 43  
retinitis pigmentosa 44  
retinitis pigmentosa 45  
retinitis pigmentosa 46  
retinitis pigmentosa 47  
retinitis pigmentosa 48  
retinitis pigmentosa 49  
retinitis pigmentosa 50  
retinitis pigmentosa 51  
retinitis pigmentosa 54  
retinitis pigmentosa 55  
retinitis pigmentosa 56  
retinitis pigmentosa 57  
retinitis pigmentosa 58  
retinitis pigmentosa 59  
retinitis pigmentosa 6 
retinitis pigmentosa 60  
retinitis pigmentosa 61  
retinitis pigmentosa 62  
retinitis pigmentosa 63 
retinitis pigmentosa 66  
retinitis pigmentosa 67  
retinitis pigmentosa 68  
retinitis pigmentosa 69  
retinitis pigmentosa 7  
Retinitis Pigmentosa 7 with Bull'S-Eye Maculopathy  
Retinitis Pigmentosa 7, Digenic  
retinitis pigmentosa 70  
retinitis pigmentosa 71  
retinitis pigmentosa 72  
retinitis pigmentosa 73  
retinitis pigmentosa 74  
retinitis pigmentosa 75  
Retinitis Pigmentosa 76  
retinitis pigmentosa 77  
Retinitis Pigmentosa 78  
Retinitis Pigmentosa 79  
Retinitis Pigmentosa 80  
retinitis pigmentosa 81  
Retinitis Pigmentosa 83  
Retinitis Pigmentosa 84  
Retinitis Pigmentosa 85  
retinitis pigmentosa 9  
RETINITIS PIGMENTOSA AND ERYTHROCYTIC MICROCYTOSIS  
Retinitis Pigmentosa Inversa with Deafness 
retinitis pigmentosa with or without situs inversus  
Retinitis Pigmentosa with Paraarteriolar Preservation Of Retinal Pigment Epithelium 
retinitis pigmentosa Y-linked 
Retinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism 
Retinitis Pigmentosa, Late-Onset Dominant  
Rhizomelic Dysplasia, Scoliosis, and Retinitis Pigmentosa 
Rhizomelic Skeletal Dysplasia with Retinitis Pigmentosa 
RHYNS Syndrome  
Rod-Cone Dystrophy, Sensorineural Deafness, and Fanconi-Type Renal Dysfunction 
Rodrigues Blindness 
Rothmund-Thomson syndrome +   
Santos Syndrome 
Schinzel-Giedion Syndrome  
Senior-Loken Syndrome 4  
Severe Mental Retardation, with Spasticity and Pigmentary Tapetoretinal Degeneration 
SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES  
Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis  
short-rib thoracic dysplasia 9 with or without polydactyly  
Sjogren-Larsson syndrome +   
Skin Fragility-Woolly Hair Syndrome  
Spastic Quadriplegia, Retinitis Pigmentosa, and Mental Retardation 
Spondyloepimetaphyseal Dysplasia with Abnormal Dentition 
Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy  
Steatocystoma Multiplex with Natal Teeth 
Stiff Skin Syndrome  
Storm Syndrome 
superficial mycosis +  
Supernumerary Tooth +  
Systemic Hyalinosis  
Tapetoretinal Degeneration with Ataxia 
Taurodontism +  
Taurodontism, Microdontia, and Dens Invaginatus 
Teebi Kaurah Syndrome 
Teeth Noneruption of with Maxillary Hypoplasia and Genu Valgum 
Teeth, Odd Shapes of 
Temple-Baraitser syndrome  
temtamy preaxial brachydactyly syndrome  
tinea capitis +  
Tonoki Syndrome 
tooth agenesis +   
tooth and nail syndrome  
Total Anonychia with Microcephaly 
Tricho-Dento-Osseous Syndrome  
Tricho-Dento-Osseous Syndrome 1 
Trichodysplasia-Xeroderma 
Trichohepatoenteric Syndrome +   
Trichohepatoneurodevelopmental Syndrome  
TRICHOMEGALY  
trichorhinophalangeal syndrome type I  
trichorhinophalangeal syndrome type III  
Trichostasis Spinulosa 
Trichothiodystrophy Syndromes +   
Ulnar Hypoplasia with Mental Retardation 
Uncombable Hair Syndrome +   
Usher syndrome +   
Vohwinkel Syndrome, Variant Form  
Weyers Acrofacial Dysostosis  
White Forelock with Malformations 
Woolly Hair, Autosomal Recessive +   
X-linked cone-rod dystrophy 1  
X-linked cone-rod dystrophy 2 
X-linked cone-rod dystrophy 3  
X-linked ichthyosis +   
X-Linked Retinitis Pigmentosa, and Sinorespiratory Infections, with or without Deafness  
xeroderma pigmentosum +   
yellow nail syndrome +  
Zazam Sheriff Phillips Syndrome 
Zori Stalker Williams Syndrome 

Synonyms
Primary IDs: MESH:C564934 ;   RDO:0013726

paths to the root

NHLBI Logo

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