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Ontology Browser

Term:
Cleft Palate with Ankyloglossia (DOID:9000786)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (0) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
cleft palate +     
tongue disease +     
46,XY sex reversal 2  
Aase Smith Syndrome 
Abruzzo-Erickson syndrome  
Achromatopsia Incomplete, X-Linked 
Acromegaloid Features, Overgrowth, Cleft Palate, and Hernia 
Aicardi syndrome 
alpha-thalassemia myelodysplasia syndrome  
Alzheimer's disease 16 
AMME complex  
androgen insensitivity syndrome +   
Anencephaly and Spina Bifida X-Linked 
angioma serpiginosum +  
Ankyloblepharon Filiforme Adnatum  
ankyloblepharon-ectodermal defects-cleft lip/palate syndrome  
ankyloglossia  
Arthrogryposis, Cleft Palate, Craniosynostosis, and Impaired Intellectual Development  
Arthrogryposis, X-Linked, Type V 
Aughton Syndrome 
Baetz-Greenwalt syndrome 
Bamforth-Lazarus syndrome  
Baraitser Rodeck Garner syndrome 
Basel-Vanagaite-Smirin-Yosef syndrome  
blepharocheilodontic syndrome +   
Bornholm Eye Disease 
Branchial Arch Syndrome X-Linked 
Bresheck/Bresek Syndrome 
Bullous Dystrophy, Hereditary Macular Type 
cataract 40  
CEREBRAL-CEREBELLAR-COLOBOMA SYNDROME, X-LINKED  
Choroideremia +   
Chromosome Xq28 Duplication Syndrome 
Cleft Lip with or without Cleft Palate, Nonsyndromic, 7 
Cleft Palate with Ankyloglossia  
Cleft Palate, Cardiac Defect, Genital Anomalies, and Ectrodactyly 
cleft palate, cardiac defects, and intellectual disabillity  
Cleft Palate, Deafness, and Oligodontia 
Cleft Palate, Midfacial Hypoplasia, Triangular Facies, and Sensorineural Hearing Loss 
Cleft Palate, Proliferative Retinopathy, and Developmental Delay  
Cleft Palate, Psychomotor Retardation, and Distinctive Facial Features  
cleft soft palate  
Coloboma of Macula and Skeletal Anomalies 
combined T cell and B cell immunodeficiency +   
Cone Dystrophy, X-Linked, with Tapetal-like Sheen 
Congenital Adrenal Hypoplasia with Precocious Puberty 
Congenital Alopecia X-Linked 
congenital bilateral absence of vas deferens +   
Congenital Heart Defects, X-Linked +   
Congenital Hydronephrosis, with Cleft Palate, Characteristic Facies, Hypotonia, and Mental Retardation 
congenital hypogammaglobulinemia 
congenital nystagmus 1  
Congenital Ptosis, Hereditary 2 
Congenital Symmetric Circumferential Skin Creases +   
corpus callosum agenesis-abnormal genitalia syndrome  
Craniofacioskeletal Syndrome 
Craniosynostosis Mental Retardation Clefting Syndrome 
Crumpled Helices and Small Mouth 
Deafness, High-Frequency Sensorineural, X-Linked 
deafness-intellectual disability, Martin-Probst type syndrome  
Diamond-Blackfan Anemia with Microtia and Cleft Palate 
Dilated Cardiomyopathy 3A  
distal arthrogryposis type 3  
Dyssegmental Dysplasia, Rolland-Desbuquois Type 
early infantile epileptic encephalopathy 8  
early infantile epileptic encephalopathy 9  
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1 
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3  
Ectrodactyly-Cleft Palate Syndrome 
EEC syndrome +   
Emanuel Syndrome 
Epidermodysplasia Verruciformis, X-Linked 
Episodic Muscle Weakness, X-Linked 
External Ophthalmoplegia and Myopia 
Fabry disease +   
Facial Dysmorphism, Cleft Palate, Hearing Loss, and Camptodactyly 
Faciocardiorenal Syndrome 
Familial Lissencephaly with Cleft Palate and Cerebellar Hypoplasia 
favism  
Feingold Trainer Syndrome 
Fetal Akinesia Syndrome, X-Linked 
fissured tongue +  
Frontonasal Dysplasia 3  
Genito Palato Cardiac Syndrome 
Glossalgia 
glossitis +  
Glossoptosis 
glycogen storage disease VIII 
hairy tongue +  
Halal Syndrome 
Hardikar Syndrome 
Hay Wells Syndrome Recessive Type 
Ho Kaufman Mcalister Syndrome 
Hodgkin Disease, X-Linked Pseudoautosomal 
Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate  
Holzgreve-Wagner-Rehder syndrome 
Hydrocephalus with Cerebellar Agenesis 
hypertelorism, microtia, facial clefting syndrome 
Hypertrichosis Congenital Generalized X-Linked 
hypertrophy of tongue papillae 
Hypodontia Oligodontia with Orofacial Cleft 
Hypospadias 1, X-Linked  
Hypospadias 2, X-Linked  
Hypotrichosis, Progressive Patterned Scalp, with Wiry Hair, Onycholysis, and Cleft Lip/Palate 
Iida Kannari Syndrome 
Intracranial Berry Aneurysm 5 
isolated cleft palate  
Isolated Microphthalmia with Coloboma 1 
Isolated Noncompaction of the Ventricular Myocardium +   
Kallmann Syndrome 2 with Cleft Lip or Palate 
Kapur Toriello Syndrome 
Kniest dysplasia  
Kuster Syndrome 
Ladda Zonana Ramer syndrome 
Larsen syndrome  
Leigh Syndrome, X-Linked  
Lowry Maclean syndrome 
Macroglossia +   
Macrosomia with Lethal Microphthalmia 
Macular Dystrophy, X-Linked +   
Martinez Monasterio Pinheiro Syndrome 
McLeod syndrome  
McPherson Clemens Syndrome 
Meester-Loeys syndrome  
Melnick-Needles syndrome  
Membranoproliferative Glomerulonephritis, X-Linked 
Mental Retardation, Skeletal Dysplasia, and Abducens Palsy 
Mental Retardation, X-Linked +   
Microcephaly Microcornea Syndrome Seemanova Type 
Microcephaly, Corpus Callosum Dysgenesis and Cleft Lip-Palate 
Microtia, Hearing Impairment, and Cleft Palate  
Midline Defects, X-Linked 
Multiple Epiphyseal Dysplasia with Robin Phenotype 
Multiple Pterygium Syndrome, X-Linked 
Myopia 1 
Myopia 13 
Myopia 26, X-Linked, Female-Limited  
Native American myopathy  
NEMO Mutation with Immunodeficiency 
Neural Tube Defects X-Linked 
Nystagmus 5, Infantile Periodic Alternating 
Oculopalatocerebral Syndrome 
Ogden syndrome  
Omphalocele, Cleft Palate Syndrome Lethal 
Opitz GBBB syndrome type I  
optic atrophy 2 
ornithine carbamoyltransferase deficiency  
ovarian dysgenesis 2  
Palant Cleft Palate Syndrome 
PARC Syndrome 
Parkinson's Disease 12 
Partial Agenesis of Corpus Callosum, X-Linked  
Periventricular Nodular Heterotopia 4  
Periventricular Nodular Heterotopia 7  
Periventricular Nodular Heterotopia, with Frontometaphyseal Dysplasia 
Piepkorn Karp Hickok syndrome 
Pilotto Syndrome 
popliteal pterygium syndrome +   
Premature Ovarian Failure 2a  
Progressive Muscular Dystrophy, Pectorodorsal 
Prostate Cancer, Hereditary, X-Linked 1 
Prostate Cancer, Hereditary, X-Linked 2 
Radial Ray Deficiency, X-Linked 
Radiation Sensitivity of Natural Killer Activity 
Radius Absent Anogenital Anomalies 
Raine Syndrome  
Rapp-Hodgkin syndrome  
Reardon Hall Slaney syndrome 
reducing body myopathy 1B  
Reticuloendotheliosis, X-Linked 
retinitis pigmentosa 2  
retinitis pigmentosa 24 
retinitis pigmentosa 3  
retinitis pigmentosa 34 
retinitis pigmentosa 6  
Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked  
Rosselli-Gulienetti Syndrome 
Russell-Silver Syndrome, X-Linked 
Sakoda Complex 
Samson Viljoen Syndrome 
Say Syndrome 
Schilbach-Rott Syndrome 
Schrander-Stumpel Theunissen Hulsmans Syndrome 
Selective Tooth Agenesis with Orofacial Cleft 
Selective Tooth Agenesis, X-Linked, 1  
Seres-Santamaria Arimany Muniz Syndrome 
Sketetal Dysplasia Coarse Facies Mental Retardation  
Spina Bifida, X-Linked 
split hand-foot malformation 2 
Spondyloepiphyseal Dysplasia with Coronal Craniosynostosis, Cataracts, Cleft Palate, and Mental Retardation 
Spondylometaphyseal Dysplasia, X-Linked 
Surfactant Metabolism Dysfunction, Pulmonary, 4  
syndromic microphthalmia 13  
TARP syndrome  
terminal osseous dysplasia  
Testicular Germ Cell Tumor 1 
Thrombocythemia, X-Linked 
Thrombocytopenia 1  
Thyroxine-Binding Globulin Deficiency +   
Tongue Neoplasms +   
Torticollis Keloids Cryptorchidism Renal Dysplasia 
uveal coloboma-cleft lip and palate-intellectual disability  
Van der Woude syndrome +   
Van der Woude Syndrome 2  
Vasquez Hurst Sotos Syndrome 
VEXAS syndrome  
Von Willebrand Disease, X-Linked Form 
Wells Jankovic Syndrome 
X Inactivation, Familial Skewed, 1  
X Inactivation, Familial Skewed, 2 
X-Linked Anemia with or without Neutropenia and/or Platelet Abnormalities  
X-Linked Anemia without Thrombocytopenia 
X-linked cardiac valvular dysplasia  
X-linked cleft palate with or without ankyloglossia  
X-linked cone-rod dystrophy 1  
X-linked cone-rod dystrophy 2 
X-linked congenital myopathy with fiber-type disproportion 
X-linked dilated cardiomyopathy  
X-linked dominant disease +   
X-linked epilepsy with variable learning disabilities and behavior disorders  
X-linked exudative vitreoretinopathy 2  
X-linked hereditary ataxia +   
X-Linked Hydrocephalus +   
X-Linked Hypogammaglobulinemia  
X-linked hypoparathyroidism 
X-Linked Immunodeficiency with Deficiency of 115,000 Dalton Surface Glycoprotein 
X-Linked Modifier for Neurofunctional Defects 
X-linked nonsyndromic deafness +   
X-linked panhypopituitarism  
X-linked recessive disease +   
X-linked reticulate pigmentary disorder  
X-linked retinitis pigmentosa and sinorespiratory infections  
X-linked Spondyloepimetaphyseal Dysplasia with Hypomyelinating Leukodystrophy   
X-Linked Tetra-Amelia 
X-Linked Thrombocytopenia, Intermittent  
X-Linked Thrombocytopenia, with or without Dyserythropoietic Anemia  
X-linked thrombophilia due to factor IX defect  
X-Linked Vesicoureteral Reflux 
Yim Ebbin Syndrome 
Zadik Barak Levin Syndrome 

Synonyms
Primary IDs: MESH:C564442 ;   RDO:0013406

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