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

Ontology Browser

Term:
Thumb Deformity, Alopecia, Pigmentation Anomaly (DOID:9002703)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0)
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, 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 
Anodontia of Permanent Dentition  
Anonychia with Flexural Pigmentation 
Argyria 
atrichia with papular lesions  
autosomal dominant keratosis follicularis spinulosa decalvans 
Axenfeld-Rieger syndrome type 1  
Axenfeld-Rieger syndrome type 2 
BADS syndrome 
Basaran Yilmaz Syndrome  
Bloch-Sulzberger syndrome +   
Brachymetapody-Anodontia-Hypotrichosis-Albinoidism 
Bullous Dystrophy, Hereditary Macular Type 
Cafe-au-Lait Spots +   
Cancer, Alopecia, Pigment Dyscrasia, Onychodystrophy, and Keratoderma  
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 Syndrome with Distinctive Facial Appearance and Preaxial Polydactyly of Feet 
Ectodermal Dysplasia, Alopecia, Preaxial Polydactyly 
Ectodermal Dysplasia, Trichoodontoonychial Type 
Elejalde Disease 
Familial Focal Alopecia 
FLOTCH Syndrome 
Follicular Hamartoma, Alopecia, Cystic Fibrosis 
follicular mucinosis 
Frontonasal Dysplasia 2  
Garret Tripp Syndrome 
Gomez Lopez Hernandez Syndrome 
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 
hypohidrotic ectodermal dysplasia +   
hypomyelinating leukodystrophy 7 with or without oligodontia and-or hypogonadotropic hypogonadism  
Hypopigmentation +   
hypopigmentation of eyelid 
hypotrichosis 7  
hypotrichosis-lymphedema-telangiectasia-renal defect syndrome  
Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome 2 
ichthyosis follicularis-alopecia-photophobia syndrome 1  
Jagell Holmgren Hofer Syndrome 
Johnson Neuroectodermal Syndrome 
Kuster Majewski Hammerstein Syndrome 
Late-Onset Localized Junctional Epidermolysis Bullosa with Mental Retardation 
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  
palmoplantar keratoderma and congenital alopecia 2 
PARC Syndrome 
Patel Bixler Syndrome 
Perniola Krajewska Carnevale Syndrome 
Pigmented Purpuric Eruption 
Pinheiro Freire-Maia Miranda Syndrome 
Precocious Graying of Hair 
Red Skin Pigment Anomaly of New Guinea 
Russell-Silver Syndrome, X-Linked 
Satoyoshi Syndrome 
Scholte Syndrome 
Schopf-Schulz-Passarge syndrome  
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 
solitary median maxillary central incisor  
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 
X-linked reticulate pigmentary disorder  
xeroderma pigmentosum +   
yellow nail syndrome +  
Zadik Barak Levin Syndrome 

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

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.