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Ontology Browser

Term:
Brachymetapody-Anodontia-Hypotrichosis-Albinoidism (DOID:9001784)
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Parent Terms Term With Siblings Child Terms
Albinism +     
anodontia +     
Dwarfism +     
Eye Abnormalities +     
hypotrichosis +     
3-M syndrome +   
3MC syndrome 1  
Aarskog syndrome +   
ablepharon macrostomia syndrome  
Abuse Dwarfism Syndrome 
achondroplasia +   
acromesomelic dysplasia +   
ADULT syndrome  
Alaninuria with Microcephaly, Dwarfism, Enamel Hypoplasia, and Diabetes Mellitus 
Albinism Deafness Syndrome 
Aloi Tomasini Isaia Syndrome 
alopecia +   
Alopecia Contractures Dwarfism Mental Retardation 
Amino Aciduria with Mental Deficiency, Dwarfism, Muscular Dystrophy, Osteoporosis, and Acidosis 
anauxetic dysplasia 1  
Anauxetic Dysplasia 2  
aniridia +   
Ankyloblepharon Filiforme Adnatum 
ankyloblepharon-ectodermal defects-cleft lip/palate syndrome  
Anodontia of Permanent Dentition 
Anophthalmia +   
anterior segment mesenchymal dysgenesis +   
Astley-Kendall Syndrome 
Asymmetric Short Stature Syndrome 
Atelosteogenesis Type 3  
autosomal recessive congenital ichthyosis 11  
Axenfeld-Rieger syndrome +   
Axenfeld-Rieger syndrome type 1  
Axenfeld-Rieger syndrome type 2 
Bangstad Syndrome 
Basaran Yilmaz Syndrome  
Basel-Vanagaite-Smirin-Yosef syndrome  
Bazex-Dupre-Christol Syndrome 
Bird Headed Dwarfism Montreal Type 
blepharophimosis +   
Blue Diaper Syndrome 
Boomerang dysplasia  
Brachydactylous Dwarfism Mseleni Type 
Brachymetapody-Anodontia-Hypotrichosis-Albinoidism 
brittle cornea syndrome +   
Brunoni Syndrome 
Bullous Dystrophy, Hereditary Macular Type 
Cantu Sanchez-Corona Fragoso Syndrome 
Chemke Oliver Mallek Syndrome 
Chondrodysplasia Calcificans Metaphysealis 
Chondrodysplasia, Megarbane-Dagher-Melki Type  
chromosome 6pter-p24 deletion syndrome 
Cleft Palate, Deafness, and Oligodontia 
Cockayne syndrome +   
CODAS syndrome  
Cole-Carpenter syndrome +   
coloboma +   
COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS  
Colobomatous Macrophthalmia with Microcornea 
Congenital Erythroderma with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-IgE  
congenital hypothyroidism +   
congenital hypotrichosis with juvenile macular dystrophy  
Congenital Nephrotic Syndrome with or without Ocular Abnormalities +   
Craniofacial Anomalies and Anterior Segment Dysgenesis Syndrome  
Craniosynostosis with Ocular Abnormalities and Hallucal Defects 
Cryptophthalmos, Unilateral or Bilateral, Isolated  
De Hauwere syndrome 
De Sanctis-Cacchione Syndrome  
Deafness Oligodontia Syndrome 
Dermatoosteolysis Kirghizian Type 
Desanto-Shinawi Syndrome  
Desbuquois dysplasia +   
diastrophic dysplasia +   
Diffuse Renal Mesangial Sclerosis, with Ocular Abnormalities 
Dilated Cardiomyopathy with Woolly Hair, Keratoderma, and Tooth Agenesis  
Disproportionate Short Stature with Ptosis and Valvular Heart Lesions 
Dwarfism Stiff Joint Ocular Abnormalities 
Dwarfism Tall Vertebrae 
Dwarfism, Familial, with Muscle Spasms 
Dwarfism, Levi Type 
Dwarfism, Low-Birth-Weight Type, with Unresponsiveness to Growth Hormone 
Dyggve-Melchior-Clausen disease +   
Dysmyelinating Leukodystrophy with Oligodontia 
Dyssegmental Dysplasia with Glaucoma 
Ectodermal Dysplasia 15, Hypohidrotic/Hair Type  
Ectodermal Dysplasia, Trichoodontoonychial Type 
ECTODERMAL DYSPLASIA/SHORT STATURE SYNDROME  
Ectopia Lentis +   
Egg-Shaped Pupil 
Epidermolysis Bullosa, Late-Onset Localized Junctional, with Mental Retardation 
FACES Syndrome 
fibrochondrogenesis +   
Foveal Hypoplasia and Anterior Segment Dysgenesis  
Fraser syndrome +   
Fronto-Facio-Nasal Dysplasia 
Frontoocular Syndrome 
geroderma osteodysplasticum  
Goniodysgenesis-Mental Retardation-Short Stature Syndrome 
Growth Retardation, Alopecia, Pseudoanodontia and Optic Atrophy  
Growth Retardation, Developmental Delay, Coarse Facies, and Early Death  
Hadziselimovic Syndrome 
Hermansky-Pudlak syndrome 1  
hydrophthalmos +   
hypochondroplasia  
Hypodontia Oligodontia with Orofacial Cleft 
hypohidrotic ectodermal dysplasia +   
hypomyelinating leukodystrophy 7 with or without oligodontia and-or hypogonadotropic hypogonadism  
hypotrichosis 1  
hypotrichosis 10 
hypotrichosis 11  
hypotrichosis 12  
hypotrichosis 13  
hypotrichosis 14  
hypotrichosis 2  
hypotrichosis 3  
hypotrichosis 4  
hypotrichosis 5 
hypotrichosis 6  
hypotrichosis 7  
hypotrichosis 8  
hypotrichosis 9 
hypotrichosis and recurrent skin vesicles  
hypotrichosis of eyelid 
Hypotrichosis, Progressive Patterned Scalp, with Wiry Hair, Onycholysis, and Cleft Lip/Palate 
Hypotrichosis-Lymphedema-Telangiectasia Syndrome +   
Hypotrichosis-Osteolysis-Periodontitis-Palmoplantar Keratoderma Syndrome 
Ichthyosis, Mental Retardation, Dwarfism, and Renal Impairment 
Intellectual Developmental Disorder with Abnormal Behavior, Microcephaly, and Short Stature  
Iridogoniodysgenesis and Skeletal Anomalies 
iridogoniodysgenesis syndrome +   
isolated growth hormone deficiency +   
Joubert syndrome 1  
Joubert Syndrome 2  
Joubert syndrome 9  
Kapur Toriello Syndrome 
Kenny-Caffey Syndrome, Type 2  
Keratosis Follicularis Dwarfism Cerebral Atrophy 
Kniest dysplasia  
Laplane Fontaine Lagardere Syndrome 
Laron syndrome +   
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis 
Loucks-Innes Syndrome  
Maxillofacial Dysostosis 
Mehta Lewis Patton Syndrome 
Mental Retardation, Macrocephaly, Short Stature and Craniofacial Dysmorphism 
Mental Retardation, Short Stature, Facial Anomalies, and Joint Dislocations  
Mesomelic Dwarfism of Hypoplastic Tibia and Radius Type 
Mesomelic Dwarfism Reinhardt Pfeiffer Type 
Metatropic Dwarfism  
Metatropic Dwarfism, Type II 
Microcephalic Osteodysplastic Primordial Dwarfism +   
Microcephalic Primordial Dwarfism Toriello Type 
Microcephaly Albinism Digital Anomalies Syndrome 
MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM +   
MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH OR WITHOUT SEIZURES  
Microcornea, Glaucoma, and Absent Frontal Sinuses 
Microcornea, Myopic Chorioretinal Atrophy, and Telecanthus  
Microdontia Hypodontia Short Stature 
microphthalmia +   
Mollica Pavone Antener Syndrome 
MOMES Syndrome 
mulibrey nanism  
Nephrotic Syndrome with Ocular Anomalies 
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART  
Nicolaides Baraitser Syndrome  
Nievergelt Syndrome 
ocular albinism +   
oculoauricular syndrome  
Oculoauriculofrontonasal syndrome 
Oculocerebrocutaneous Syndrome 
oculocutaneous albinism +   
oculodentodigital dysplasia +   
Oculodentodigital Dysplasia, Autosomal Recessive  
Oculomaxillofacial Dysostosis  
Oculopalatocerebral Syndrome 
Oculorenocerebellar Syndrome 
Oligodontia-Colorectal Cancer Syndrome  
Oliver-McFarlane syndrome  
otospondylomegaepiphyseal dysplasia  
Parastremmatic Dwarfism  
Pena Shokeir Syndrome Type 2 
persistent hyperplastic primary vitreous +   
PHACE Association 
piebaldism +   
Pierson syndrome  
Pinheiro Freire-Maia Miranda Syndrome 
popliteal pterygium syndrome +   
Prepapillary Vascular Loops 
Proportionate Dwarfism, with Hip Dislocation 
Pseudodiastrophic Dysplasia 
Pupillary Membrane, Persistence of 
rapadilino syndrome  
Retinal Dysplasia +   
Robinow syndrome +   
Rombo syndrome 
Rommen Mueller Sybert Syndrome 
Rozin Hertz Goodman Syndrome 
Ruvalcaba Syndrome 
Schmid-Fraccaro Syndrome 
Schopf-Schulz-Passarge Syndrome  
Seckel Like Syndrome Type Buebel 
Seckel syndrome 1  
Seckel syndrome 2  
Seckel Syndrome 3 
Seckel syndrome 4  
Short Limb Dwarfism Al Gazali Type 
Short Stature and Facioauriculothoracic Malformations 
SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES  
SHORT STATURE WITH NONSPECIFIC SKELETAL ABNORMALITIES  
SHORT STATURE, DEVELOPMENTAL DELAY, AND CONGENITAL HEART DEFECTS  
SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES  
SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES  
Short Stature, Mental Retardation, Callosal Agenesis, Heminasal Hypoplasia, Microphthalmia, and Atypical Clefting 
SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION  
Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis  
SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY  
Short Stature-Obesity Syndrome 
Silver-Russell syndrome +   
Silverman-Handmaker type dyssegmental dysplasia  
Singh Chhaparwal Dhanda Syndrome 
Single Upper Central Incisor  
Split-Hand and Split-Foot With Hypodontia 
Spondyloepimetaphyseal Dysplasia with Hypotrichosis 
Spondyloepiphyseal Dysplasia Tarda, Toledo Type 
Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type  
Storm Syndrome 
Stromme syndrome  
Synovial Chondromatosis, Familial, with Dwarfism 
Taurodontia Absent Teeth Sparse Hair 
Thai Symphalangism Syndrome 
Thoraco Limb Dysplasia Rivera Type 
Thoracomelic Dysplasia 
Thumb Deformity, Alopecia, Pigmentation Anomaly 
tooth and nail syndrome  
torsion dystonia with onset in infancy 
Trichoodontoonychial Dysplasia 
Tryptophanuria with Dwarfism 
Weill-Marchesani syndrome +   
Weill-Marchesani-Like Syndrome  
Woolly Hair, Autosomal Recessive 3  
X-Linked Hypodontia 
Zadik Barak Levin Syndrome 

Synonyms
Exact Synonyms: Anodontia-Hypotrichosis Syndrome ;   Oculoosteocutaneous Syndrome
Primary IDs: MESH:C565893 ;   RDO:0014413

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