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Thumb Deformity, Alopecia, Pigmentation Anomaly (DOID:9002703)
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Parent Terms Term With Siblings Child Terms
alopecia +     
anodontia +     
acanthosis nigricans +   
ADULT syndrome  
Aloi Tomasini Isaia Syndrome 
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 1  
Alopecia-Mental Retardation Syndrome 2 
Alopecia-Mental Retardation Syndrome 3 
Alopecia-Mental Retardation Syndrome with Convulsions and Hypergonadotropic Hypogonadism 
Androgenetic Alopecia 2 
Androgenetic Alopecia 3 
androgenic alopecia 
Anodontia of Permanent Dentition 
Anonychia with Flexural Pigmentation 
atrichia with papular lesions  
Axenfeld-Rieger syndrome type 1  
Axenfeld-Rieger syndrome type 2 
BADS syndrome 
Basaran Yilmaz Syndrome  
Bloch-Sulzberger syndrome +   
Bullous Dystrophy, Hereditary Macular Type 
Cafe-au-Lait Spots +   
Cataract, Alopecia, Sclerodactyly 
Central Centrifugal Cicatricial Alopecia 
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy  
Cleft Palate, Deafness, and Oligodontia 
Congenital Alopecia X-Linked 
conjunctival pigmentation 
Cutaneous Telangiectasia and Cancer Syndrome, Familial  
Deafness Oligodontia Syndrome 
Dermatoosteolysis Kirghizian Type 
Dermatopathia Pigmentosa Reticularis  
Dilated Cardiomyopathy with Woolly Hair, Keratoderma, and Tooth Agenesis  
dyschromatosis symmetrica hereditaria  
dyschromatosis universalis hereditaria +   
Dysmyelinating Leukodystrophy with Oligodontia 
Ectodermal Dysplasia Alopecia Preaxial Polydactyly 
Ectodermal Dysplasia Syndrome with Distinctive Facial Appearance and Preaxial Polydactyly of Feet 
Ectodermal Dysplasia, Trichoodontoonychial Type 
Elejalde Disease 
Epidermolysis Bullosa, Late-Onset Localized Junctional, with Mental Retardation 
Familial Focal Alopecia 
FLOTCH Syndrome 
Follicular Hamartoma, Alopecia, Cystic Fibrosis 
follicular mucinosis 
Frontonasal Dysplasia 2  
Garret Tripp Syndrome 
Glomerulonephritis with Sparse Hair and Telangiectases  
Gomez Lopez Hernandez Syndrome 
Graying of Hair, Precocious 
Griscelli syndrome +   
Grouped Pigmentation of the Macula 
Growth Retardation, Alopecia, Pseudoanodontia and Optic Atrophy  
Heterochromia Iridis  
Hypergonadotropic Hypogonadism And Partial Alopecia 
Hyperpigmentation +   
Hypodontia Oligodontia with Orofacial Cleft 
hypomyelinating leukodystrophy 7 with or without oligodontia and-or hypogonadotropic hypogonadism  
Hypopigmentation +   
hypopigmentation of eyelid 
hypotrichosis 7  
Ichthyosis Follicularis Atrichia Photophobia Syndrome  
Jagell Holmgren Hofer Syndrome 
Johnson Neuroectodermal Syndrome 
Keratosis Follicularis Spinulosa Decalvans, Autosomal Dominant 
Kuster Majewski Hammerstein Syndrome 
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis 
Loose Anagen Hair Syndrome +   
Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis  
Macules Hereditary Congenital Hypopigmented and Hyperpigmented 
mandibulofacial dysostosis with alopecia  
Mehta Lewis Patton Syndrome 
Microcephaly Sparse Hair Mental Retardation Seizures 
Microdontia Hypodontia Short Stature 
Moloney Syndrome 
neonatal jaundice +   
Nisch syndrome  
Oculocerebral Hypopigmentation Syndrome Type Preus 
Oligodontia-Colorectal Cancer Syndrome  
PARC Syndrome 
Patel Bixler Syndrome 
Perniola Krajewska Carnevale Syndrome 
Pigmented Purpuric Eruption 
Pinheiro Freire-Maia Miranda Syndrome 
Red Skin Pigment Anomaly of New Guinea 
Reticulate Pigmentary Disorder, with Systemic Manifestations  
Russell-Silver Syndrome, X-Linked 
Satoyoshi Syndrome 
Scholte Syndrome 
Schopf-Schulz-Passarge Syndrome  
Single Upper Central Incisor  
Skin/Hair/Eye Pigmentation, Variation In, 1  
Skin/Hair/Eye Pigmentation, Variation In, 10  
Skin/Hair/Eye Pigmentation, Variation In, 11  
Skin/Hair/Eye Pigmentation, Variation In, 4  
Skin/Hair/Eye Pigmentation, Variation In, 5  
Skin/Hair/Eye Pigmentation, Variation In, 6  
Skin/Hair/Eye Pigmentation, Variation In, 7  
Skin/Hair/Eye Pigmentation, Variation In, 8  
Skin/Hair/Eye Pigmentation, Variation In, 9  
Slti Salem Syndrome 
Split-Hand and Split-Foot With Hypodontia 
stromal corneal pigmentation 
Symmetric Acroleukopathy 
T-cell immunodeficiency, congenital alopecia, and nail dystrophy  
Tang Hsi Ryu Syndrome 
Taurodontia Absent Teeth Sparse Hair 
telogen effluvium 
Terminal Osseous Dysplasia and Pigmentary Defects  
Thai Symphalangism Syndrome 
Thumb Deformity and Alopecia 
Thumb Deformity, Alopecia, Pigmentation Anomaly 
tooth and nail syndrome  
Urban Schosser Spohn Syndrome 
urticaria pigmentosa  
Waardenburg Syndrome Type 4 +   
White Forelock with Malformations 
Whyte Murphy Syndrome 
Woodhouse Sakati Syndrome  
Woolly Hair, Hypotrichosis, Everted Lower Lip and Outstanding Ears 
X-Linked Hypodontia 
xeroderma pigmentosum +   
yellow nail syndrome +  
Zadik Barak Levin Syndrome 

Exact Synonyms: Congenital deformity of the thumb and congenital alopecia ;   Hypotrichosis associated with congenital hypoplasia of the thumb
Primary IDs: MESH:C536904 ;   RDO:0002625

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