Ontology Browser

Term:
Bird Headed Dwarfism Montreal Type (DOID:9008368)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0)
Parent Terms Term With Siblings Child Terms
Dwarfism +     
hair disease +     
Micrognathism +     
progeria +     
3-M syndrome +   
Aarskog syndrome +   
Abuse Dwarfism Syndrome 
achondroplasia +   
Acrogeria, Gottron Type 
acromesomelic dysplasia +   
Alaninuria with Microcephaly, Dwarfism, Enamel Hypoplasia, and Diabetes Mellitus 
Alopecia Contractures Dwarfism Mental Retardation 
Amino Aciduria with Mental Deficiency, Dwarfism, Muscular Dystrophy, Osteoporosis, and Acidosis 
anauxetic dysplasia 1  
Anauxetic Dysplasia 2  
Astley-Kendall Syndrome 
Asymmetric Short Stature Syndrome 
Atelosteogenesis Type 3  
Baetz-Greenwalt syndrome 
Bamforth-Lazarus syndrome  
Bangstad Syndrome 
Bird Headed Dwarfism Montreal Type 
Bjornstad syndrome  
Boomerang dysplasia  
Brachycephaly, Trichomegaly, and Developmental Delay  
Brachydactylous Dwarfism Mseleni Type 
Brachymetapody-Anodontia-Hypotrichosis-Albinoidism 
Brunoni Syndrome 
Bullous Dystrophy, Hereditary Macular Type 
Cantu Sanchez-Corona Fragoso Syndrome 
Catatrichy 
cerebral cavernous malformation 2  
cerebral cavernous malformation 3  
Cerebrocostomandibular Syndrome  
Chondrodysplasia Calcificans Metaphysealis 
Chondrodysplasia, Megarbane-Dagher-Melki Type  
Clavicular Hypoplasia, Zygomatic Arch Hypoplasia, and Micrognathia 
Cockayne syndrome +   
Coffin-Siris syndrome +   
congenital hypothyroidism +   
Congenital Woolly Hair +   
Copper Deficiency, Familial Benign 
corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome  
Crumpled Helices and Small Mouth 
Curly Hair-Ankyloblepharon-Nail Dysplasia Syndrome  
De Sanctis-Cacchione Syndrome  
Dermoodontodysplasia 
Desbuquois dysplasia +   
diastrophic dysplasia  
Diastrophic Dysplasia, Broad Bone-Platyspondylic Variant  
dilated cardiomyopathy with woolly hair and keratoderma +   
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 +   
Dyssegmental Dysplasia with Glaucoma 
Ectodermal Dysplasia 4, Hair/Nail Type  
Ectodermal Dysplasia 9, Hair/Nail Type  
ECTODERMAL DYSPLASIA/SHORT STATURE SYNDROME  
Ectrodactyly of Lower Limbs, Congenital Heart Defect, and Micrognathia 
fibrochondrogenesis +   
FLOTCH Syndrome 
folliculitis +   
Genee-Wiedemann Syndrome  
Genito Palato Cardiac Syndrome 
Gerodermia Osteodysplastica  
Growth Retardation, Developmental Delay, Coarse Facies, and Early Death  
Hadziselimovic Syndrome 
Hairy Palms and Soles 
Hirsutism +   
Ho Kaufman Mcalister Syndrome 
hypertrichosis +   
hypochondroplasia  
hypotrichosis +   
Ichthyosis, Mental Retardation, Dwarfism, and Renal Impairment 
Intellectual Developmental Disorder with Abnormal Behavior, Microcephaly, and Short Stature  
isolated growth hormone deficiency +   
Kaler Garrity Stern Syndrome 
Katsantoni Papadakou Lagoyanni Syndrome 
Kenny-Caffey Syndrome, Type 2  
Keratosis Follicularis Dwarfism Cerebral Atrophy 
Kniest dysplasia  
Kozlowski-Krajewska Syndrome 
Laplane Fontaine Lagardere Syndrome 
Laron syndrome +   
Loucks-Innes Syndrome  
Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome  
Martinez Monasterio Pinheiro Syndrome 
Meier-Gorlin syndrome +   
Menkes disease +   
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, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM +   
MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH OR WITHOUT SEIZURES  
Milner Khallouf Gibson Syndrome 
Mollica Pavone Antener Syndrome 
monilethrix +   
mulibrey nanism  
Multiple Epiphyseal Dysplasia with Robin Phenotype 
Naxos Disease  
Nievergelt Syndrome 
Oculopalatocerebral Syndrome 
Oculotrichodysplasia 
Oliver-McFarlane Syndrome  
otospondylomegaepiphyseal dysplasia  
Parastremmatic Dwarfism  
Pedal Onychogryposis with Keratosis Plantaris and Coarse Hair 
Penttinen-Aula Syndrome  
Petty Laxova Wiedemann Syndrome 
Photosensitive Trichothiodystrophy 1  
Pili Annulati 
Pili Multigemini 
Pili Torti +  
Premature Aging Syndrome, Okamoto Type 
Progeria Short Stature Pigmented Nevi 
Progeria Syndrome, Childhood-Onset +   
Progeroid Facial Appearance with Hand Anomalies 
Progeroid Syndrome, Congenital, Petty Type  
Progeroid Syndrome, Neonatal 
Proportionate Dwarfism, with Hip Dislocation 
Pseudodiastrophic Dysplasia 
Pseudofolliculitis Barbae  
Pseudomonilethrix 
rapadilino syndrome  
Robinow syndrome +   
Rodrigues Blindness 
Rommen Mueller Sybert Syndrome 
Ruijs-Aalfs Syndrome  
Ruvalcaba Churesigaew Myhre Syndrome 
Ruvalcaba Syndrome 
Schweitzer Kemink Graham 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, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY  
Short Stature-Obesity Syndrome 
Silver-Russell syndrome +   
Silverman-Handmaker type dyssegmental dysplasia  
Singh Chhaparwal Dhanda Syndrome 
Skin Fragility-Woolly Hair Syndrome  
split hand-foot malformation 3  
Spondyloepiphyseal Dysplasia Tarda, Toledo Type 
Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type  
superficial mycosis +  
Synovial Chondromatosis, Familial, with Dwarfism 
Thoraco Limb Dysplasia Rivera Type 
Thoracomelic Dysplasia 
tinea capitis +  
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 
Trigonobrachycephaly, Bulbous Bifid Nose, Micrognathia, and Abnormalities of the Hands and Feet 
Tryptophanuria with Dwarfism 
Uncombable Hair Syndrome +   
Weill-Marchesani syndrome +   
Weill-Marchesani-Like Syndrome  
White Forelock with Malformations 
Woolly Hair, Autosomal Recessive +   
Yunis-Varon syndrome  

Synonyms
Exact Synonyms: Bird-headed dwarfism with features of premature senility
Primary IDs: MESH:C535448 ;   RDO:0000565

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