Cleft palate, and Pancytopenia

Diseases related with Cleft palate and Pancytopenia

In the following list you will find some of the most common rare diseases related to Cleft palate and Pancytopenia that can help you solving undiagnosed cases.


Top matches:

Medium match DIAMOND-BLACKFAN ANEMIA 1; DBA1


Diamond-Blackfan anemia (DBA) is an inherited red blood cell aplasia that usually presents in the first year of life. The main features are normochromic macrocytic anemia, reticulocytopenia, and nearly absent erythroid progenitors in the bone marrow. Patients show growth retardation, and approximately 30 to 50% have craniofacial, upper limb, heart, and urinary system congenital malformations. The majority of patients have increased mean corpuscular volume, elevated erythrocyte adenosine deaminase activity, and persistence of hemoglobin F. However, some DBA patients do not exhibit these findings, and even in the same family, symptoms can vary between affected family members (summary by Landowski et al., 2013). Genetic Heterogeneity of Diamond-Blackfan AnemiaA locus for DBA (DBA2 ) has been mapped to chromosome 8p23-p22. Other forms of DBA include DBA3 (OMIM ), caused by mutation in the RPS24 gene (OMIM ) on 10q22; DBA4 (OMIM ), caused by mutation in the RPS17 gene (OMIM ) on 15q; DBA5 (OMIM ), caused by mutation in the RPL35A gene (OMIM ) on 3q29; DBA6 (OMIM ), caused by mutation in the RPL5 gene (OMIM ) on 1p22.1; DBA7 (OMIM ), caused by mutation in the RPL11 gene (OMIM ) on 1p36; DBA8 (OMIM ), caused by mutation in the RPS7 gene (OMIM ) on 2p25; DBA9 (OMIM ), caused by mutation in the RPS10 gene (OMIM ) on 6p; DBA10 (OMIM ), caused by mutation in the RPS26 (OMIM ) gene on 12q; DBA11 (OMIM ), caused by mutation in the RPL26 gene (OMIM ) on 17p13; DBA12 (OMIM ), caused by mutation in the RPL15 gene (OMIM ) on 3p24; DBA13 (OMIM ), caused by mutation in the RPS29 gene (OMIM ) on 14q; DBA14 (OMIM ), caused by mutation in the TSR2 gene (OMIM ) on Xp11; DBA15 (OMIM ), caused by mutation in the RPS28 gene (OMIM ) on 19p13; DBA16 (OMIM ), caused by mutation in the RPL27 gene (OMIM ) on chromosome 17q21; and DBA17 (OMIM ), caused by mutation in the RPS27 gene (OMIM ) on chromosome 1q21.Boria et al. (2010) reviewed the molecular basis of Diamond-Blackfan anemia, emphasizing that it is a disorder of defective ribosome synthesis.Gazda et al. (2012) completed a large-scale screen of 79 ribosomal protein genes in families with Diamond-Blackfan anemia and stated that of the 10 known DBA-associated genes, RPS19 accounts for approximately 25% of patients; RPS24, 2%; RPS17, 1%; RPL35A, 3.5%; RPL5, 6.6%; RPL11, 4.8%; RPS7, 1%; RPS10, 6.4%; RPS26, 2.6%; and RPL26, 1%. Gazda et al. (2012) stated that in total these mutations account for approximately 54% of all DBA patients.In a study of 98 Japanese patients with DBA, Wang et al. (2015) detected probable causative mutations or large deletions in ribosomal protein genes in 56 (55%) of the patients, involving the RPS19 gene in 16 patients, RPL5 in 12, RPS17 in 7, RPL35A in 7, RPL11 in 5, and RPS26 in 4; RPS7, RPS10, RPL27, and RPS27 were each mutated in 1 patient.

DIAMOND-BLACKFAN ANEMIA 1; DBA1 Is also known as red cell aplasia, pure, hereditary|anemia, congenital erythroid hypoplastic|dba|blackfan-diamond syndrome|anemia, congenital hypoplastic, of blackfan and diamond|bds|erythrogenesis imperfecta|aase-smith syndrome ii|aregenerative anemia, chronic congenital

Related symptoms:

  • Intellectual disability
  • Short stature
  • Microcephaly
  • Growth delay
  • Hypertelorism


SOURCES: OMIM MENDELIAN

More info about DIAMOND-BLACKFAN ANEMIA 1; DBA1

Medium match SECKEL SYNDROME 1; SCKL1


Seckel syndrome is a rare autosomal recessive disorder characterized by intrauterine growth retardation, dwarfism, microcephaly with mental retardation, and a characteristic 'bird-headed' facial appearance (Shanske et al., 1997). Genetic Heterogeneity of Seckel SyndromeOther forms of Seckel syndrome include SCKL2 (OMIM ), caused by mutation in the RBBP8 gene (OMIM ) on chromosome 18q11; SCKL4 (OMIM ), caused by mutation in the CENPJ gene (OMIM ) on chromosome 13q12; SCKL5 (OMIM ), caused by mutation in the CEP152 gene (OMIM ) on chromosome 15q21; SCKL6 (OMIM ), caused by mutation in the CEP63 gene (OMIM ) on chromosome 3q22; SCKL7 (OMIM ), caused by mutation in the NIN gene (OMIM ) on chromosome 14q22; SCKL8 (OMIM ), caused by mutation in the DNA2 gene (OMIM ) on chromosome 10q21; SCKL9 (OMIM ), caused by mutation in the TRAIP gene (OMIM ) on chromosome 3p21; and SCKL10 (OMIM ), caused by mutation in the NSMCE2 gene (OMIM ) on chromosome 8q24.The report of a Seckel syndrome locus on chromosome 14q, designated SCKL3, by Kilinc et al. (2003) was found to be in error; see HISTORY.

SECKEL SYNDROME 1; SCKL1 Is also known as bird-headed dwarfism|nanocephalic dwarfism|sckl|microcephalic primordial dwarfism i|seckel-type dwarfism

Related symptoms:

  • Intellectual disability
  • Seizures
  • Short stature
  • Microcephaly
  • Scoliosis


SOURCES: OMIM MENDELIAN

More info about SECKEL SYNDROME 1; SCKL1

Medium match BALLER-GEROLD SYNDROME


Baller-Gerold syndrome is characterized by the association of coronal craniosynostosis with radial ray anomalies (oligodactyly, aplasia or hypoplasia of the thumb, aplasia or hypoplasia of the radius).

BALLER-GEROLD SYNDROME Is also known as craniosynostosis-radial aplasia syndrome|craniosynostosis with radial defects

Related symptoms:

  • Intellectual disability
  • Seizures
  • Short stature
  • Hearing impairment
  • Scoliosis


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about BALLER-GEROLD SYNDROME

Mendelian

Too many results?
We can help you with your rare disease diagnosis.

Learn more

Other less relevant matches:

Medium match THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR


The thrombocytopenia-absent radius syndrome (TAR) is characterized by reduction in the number of platelets and absence of the radius; preservation of the thumb distinguishes TAR from other syndromes that combine blood abnormalities with absence of the radius, such as Fanconi anemia (see {227650}). Individuals with TAR have low numbers of megakaryocytes, platelet precursor cells that reside in bone marrow, and frequently present with bleeding episodes in the first year of life that diminish in frequency and severity with age. The severity of skeletal anomalies varies from absence of radii to virtual absence of upper limbs, with or without lower limb defects such as malformations of the hip and knee (summary by Albers et al., 2012).

THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR Is also known as tar syndrome|chromosome 1q21.1 deletion syndrome, 200-kb

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Hearing impairment


SOURCES: ORPHANET OMIM MENDELIAN

More info about THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR

Low match FANCONI ANEMIA


Fanconi anemia (FA) is a hereditary DNA repair disorder characterized by progressive pancytopenia with bone marrow failure, variable congenital malformations and predisposition to develop hematological or solid tumors.

FANCONI ANEMIA Is also known as fanconi pancytopenia|fanconi anemia|fa

Related symptoms:

  • Intellectual disability
  • Global developmental delay
  • Short stature
  • Hearing impairment
  • Microcephaly


SOURCES: OMIM ORPHANET MENDELIAN

More info about FANCONI ANEMIA

Low match METHYLMALONIC ACIDEMIA WITH HOMOCYSTINURIA TYPE CBLF


cblF type methylmalonic acidemia with homocystinuria is a form of methylmalonic acidemia with homocystinuria (see this term), an inborn error of vitamin B12 (cobalamin) metabolism characterized by megaloblastic anemia, lethargy, failure to thrive, developmental delay, intellectual deficit and seizures.

METHYLMALONIC ACIDEMIA WITH HOMOCYSTINURIA TYPE CBLF Is also known as cobalamin, defect in lysosomal release of|cobalamin f defect|combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblf|cblf|vitamin b12 storage disease|vitamin b12 lysosomal release defect|methylmalonic aciduria due to vitamin b12-rele

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Ataxia


SOURCES: ORPHANET MESH OMIM MENDELIAN

More info about METHYLMALONIC ACIDEMIA WITH HOMOCYSTINURIA TYPE CBLF

Low match NEURODEVELOPMENTAL DISORDER WITH BRAIN, LIVER, AND LUNG ABNORMALITIES; NEDBLLA


Related symptoms:

  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Growth delay
  • Failure to thrive


SOURCES: OMIM MENDELIAN

More info about NEURODEVELOPMENTAL DISORDER WITH BRAIN, LIVER, AND LUNG ABNORMALITIES; NEDBLLA

Low match DIAMOND-BLACKFAN ANEMIA 11; DBA11


Diamond-Blackfan anemia (DBA) is an inherited red blood cell aplasia that usually presents in the first year of life. The main features are normochromic macrocytic anemia, reticulocytopenia, and nearly absent erythroid progenitors in the bone marrow. Patients show growth retardation, and approximately 30 to 50% have craniofacial, upper limb, heart, and urinary system congenital malformations. The majority of patients have increased mean corpuscular volume, elevated erythrocyte adenosine deaminase activity, and persistence of hemoglobin F. However, some DBA patients do not exhibit these findings, and even in the same family, symptoms can vary between affected family members (summary by Landowski et al., 2013).For a discussion of genetic heterogeneity of Diamond-Blackfan anemia, see DBA1 (OMIM ).

Related symptoms:

  • Short stature
  • Growth delay
  • Cleft palate
  • Anemia
  • Neutropenia


SOURCES: OMIM MENDELIAN

More info about DIAMOND-BLACKFAN ANEMIA 11; DBA11

Low match SYNDROMIC DIARRHEA


Syndromic diarrhea (SD), or tricho-hepato-enteric syndrome (THE), is a severe congenital enteropathy manifesting as intractable diarrhea in the first month of life with failure to thrive and associated with facial dysmorphism, hair abnormalities, and, in some cases, immune disorders and intrauterine growth restriction.

SYNDROMIC DIARRHEA Is also known as trichohepatoenteric syndrome|tricho-hepato-enteric syndrome|diarrhea, fatal infantile, with trichorrhexis nodosa|sd/the|the syndrome|phenotypic diarrhea|diarrhea, syndromic|syndromic diarrhea/tricho-hepato-enteric syndrome

Related symptoms:

  • Intellectual disability
  • Global developmental delay
  • Short stature
  • Growth delay
  • Hypertelorism


SOURCES: OMIM ORPHANET MENDELIAN

More info about SYNDROMIC DIARRHEA

Low match FANCONI ANEMIA, COMPLEMENTATION GROUP L; FANCL


Fanconi anemia (FA) is a clinically and genetically heterogeneous disorder that causes genomic instability. Characteristic clinical features include developmental abnormalities in major organ systems, early-onset bone marrow failure, and a high predisposition to cancer. The cellular hallmark of FA is hypersensitivity to DNA crosslinking agents and high frequency of chromosomal aberrations pointing to a defect in DNA repair (summary by Deakyne and Mazin, 2011).For additional general information and a discussion of genetic heterogeneity of Fanconi anemia, see {227650}.

Related symptoms:

  • Global developmental delay
  • Growth delay
  • Hypertelorism
  • Neoplasm
  • Abnormal facial shape


SOURCES: OMIM MENDELIAN

More info about FANCONI ANEMIA, COMPLEMENTATION GROUP L; FANCL

Top 5 symptoms//phenotypes associated to Cleft palate and Pancytopenia

Symptoms // Phenotype % cases
Anemia Very Common - Between 80% and 100% cases
Growth delay Common - Between 50% and 80% cases
Intellectual disability Common - Between 50% and 80% cases
Short stature Common - Between 50% and 80% cases
Intrauterine growth retardation Common - Between 50% and 80% cases
Mendelian

Accelerate your rare disease diagnosis with us

Learn more

Other less frequent symptoms

Patients with Cleft palate and Pancytopenia. may also develop some of the following symptoms:

Common Symptoms - More than 50% cases


Abnormal heart morphology

Uncommon Symptoms - Between 30% and 50% cases


Thrombocytopenia

Common Symptoms - More than 50% cases


High palate

Uncommon Symptoms - Between 30% and 50% cases


Global developmental delay Strabismus Leukemia Hypoplasia of the radius Seizures Ventricular septal defect Micrognathia Hypertelorism Absent thumb Chromosome breakage Failure to thrive Abnormality of the skeletal system Microtia Abnormal cardiac septum morphology Neutropenia Bone marrow hypocellularity Scoliosis Small for gestational age Downslanted palpebral fissures Low-set ears Aplastic anemia Clinodactyly of the 5th finger Macrocytic anemia Acute myeloid leukemia Reticulocytopenia Abnormality of the kidney Hip dislocation Facial asymmetry Hearing impairment Epicanthus Frontal bossing Hydrocephalus Anal atresia Tracheoesophageal fistula Hypoplasia of the ulna Absent radius Depressed nasal bridge Tetralogy of Fallot Abnormal facial shape Abnormality of the liver Myeloid leukemia Proptosis Short thumb Microcephaly Edema Myelodysplasia Atrial septal defect

Rare Symptoms - Less than 30% cases


Cirrhosis Vomiting Glaucoma Hernia Abnormal vertebral morphology Lymphoma Elevated hepatic transaminase Bifid uvula Retrognathia Broad forehead Skin rash Hydronephrosis Cleft lip Carpal synostosis Narrow mouth Brachycephaly Prominent forehead Agenesis of corpus callosum Abnormality of cardiovascular system morphology Lethargy Motor delay Nystagmus Hypoalbuminemia Acute monocytic leukemia Wide nasal bridge Narrow face Aplasia/Hypoplasia of the radius Abnormality of the eye Rectovaginal fistula Horseshoe kidney Microphthalmia Hepatomegaly Renal agenesis Neoplasm Ataxia Oligohydramnios Cafe-au-lait spot Leukopenia Meckel diverticulum Abnormal eyelid morphology Fatigue Spina bifida Abnormal localization of kidney Abnormality of chromosome stability Short neck Sepsis Finger syndactyly Anteverted nares Ptosis Cataract Bilateral radial aplasia Generalized hypotonia Feeding difficulties Aciduria Sloping forehead Cerebellar vermis hypoplasia Congestive heart failure Cryptorchidism Triphalangeal thumb Prominent nose Hypoplastic anemia Hypospadias Partial duplication of thumb phalanx Depressed nasal ridge Severe short stature Upslanted palpebral fissure Abnormality of the pinna Postnatal growth retardation Coarctation of aorta Premature birth Pulmonic stenosis Anemia of inadequate production Increased mean corpuscular volume Pes planus 11 pairs of ribs Thrombocytosis Osteosarcoma Deficient excision of UV-induced pyrimidine dimers in DNA Abnormal renal morphology Dolichocephaly Duodenal stenosis Primary hypothyroidism Peripheral pulmonary artery stenosis Abnormality of nervous system morphology Abnormal aortic morphology Trichorrhexis nodosa Abnormal aortic valve morphology Abnormal thrombocyte morphology Toe syndactyly Increased mean platelet volume Abnormality of the hypothalamus-pituitary axis Abnormality of the foot Intermittent diarrhea Abnormality of femur morphology Bicornuate uterus Abnormality of the thumb Duplicated collecting system Low-grade fever Anemic pallor Large forehead Irritability Prolonged G2 phase of cell cycle Abnormal carotid artery morphology Almond-shaped palpebral fissure Underdeveloped supraorbital ridges Compensated hypothyroidism Woolly hair Villous atrophy Humoral immunodeficiency Absent testis Abnormality of the pancreas Chromosomal breakage induced by crosslinking agents Decreased fertility in males Clubbing of toes Complete duplication of thumb phalanx Neoplasm of head and neck Aplasia/Hypoplasia of the iris Hypermethioninemia Abnormality of the uterus Abnormality of the testis Type I diabetes mellitus Reduced bone mineral density Hypopigmented skin patches Renal hypoplasia/aplasia Cranial nerve paralysis Secretory diarrhea Azoospermia Hypergalactosemia Hypergonadotropic hypogonadism Abnormality of the urinary system Insulin resistance Forearm undergrowth Telangiectasia Recurrent urinary tract infections Aganglionic megacolon Abnormality of the genital system Choanal atresia Short palpebral fissure Abnormality of vision Hypopigmentation of the skin Abnormality of the upper limb Irregular hyperpigmentation B-cell lymphoma Arteriovenous malformation Abnormality of the ulna Astigmatism Intractable diarrhea Hearing abnormality Aplasia/Hypoplasia of fingers External ear malformation Abnormality of blood and blood-forming tissues Hyperinsulinemia Multiple cafe-au-lait spots Vertigo Abnormality of skin pigmentation Hydroureter Ectopic kidney Squamous cell carcinoma Glucose intolerance Bruising susceptibility Aplasia/Hypoplasia of the uvula Jaundice Pyridoxine-responsive sideroblastic anemia Depressed nasal tip Tachypnea Renal hypoplasia Dry skin Hepatic failure Esophageal atresia Hypocalcemia Decreased liver function Micropenis Abnormal lung morphology Portal hypertension Cholestasis Wide nose Abnormalities of placenta or umbilical cord Hypertrophic cardiomyopathy Ascites Fine hair Hepatic steatosis Chronic diarrhea Abnormality of eye movement Delayed puberty Rickets Cough Stenosis of the external auditory canal Polyhydramnios Osteoporosis Immunodeficiency Respiratory tract infection Long philtrum Diarrhea Wide mouth Cognitive impairment Forearm reduction defects Radioulnar synostosis Interstitial pulmonary abnormality Atresia of the external auditory canal Bicuspid aortic valve Full cheeks Small scrotum Vitamin A deficiency Sparse hair Anasarca Vitamin D deficiency Bile duct proliferation Hepatic fibrosis Joint laxity Abnormality of the preputium Psychosis Curly hair Methylmalonic aciduria Stomatitis Juvenile rheumatoid arthritis Megaloblastic anemia Iron deficiency anemia Rheumatoid arthritis Incoordination Abnormality of the skin Methylmalonic acidemia Large placenta Developmental regression Feeding difficulties in infancy Arthritis Thin upper lip vermilion Acidosis Muscular hypotonia Abnormality of iron homeostasis Galactosuria Homocystinuria Glossitis Abnormality of the hair Respiratory insufficiency Aortic regurgitation Deeply set eye Hypoglycemia Osteopenia Gastroesophageal reflux Inguinal hernia Recurrent upper respiratory tract infections Recurrent infections Cerebral atrophy Renal cortical microcysts Hyperhomocystinemia Hypertension Cystathioninemia Cystathioninuria Decreased methionine synthase activity Decreased adenosylcobalamin Megaloblastic bone marrow Brittle hair Decreased methylcobalamin Abnormality of the immune system Increased serum iron Hemangioma Carcinoma Selective tooth agenesis Optic atrophy Myopia Hypoplasia of proximal fibula Large basal ganglia Hypoplasia of proximal radius Abnormal finger flexion creases Ivory epiphyses Small anterior fontanelle Lumbar scoliosis Abnormal cortical gyration Short nose Abnormally large globe Cone-shaped epiphyses of the phalanges of the hand Severe intrauterine growth retardation Proportionate short stature Dislocated radial head Clitoral hypertrophy Patent foramen ovale Sandal gap Narrow palate Behavioral abnormality Conductive hearing impairment Dental crowding Abnormality of the metacarpal bones Fibular hypoplasia Oligodactyly Short humerus Aplasia/Hypoplasia of the thumb Anteriorly placed anus Narrow nasal bridge Hallux valgus Trigonocephaly Failure to thrive in infancy Spina bifida occulta Low-set, posteriorly rotated ears Large fontanelles Renal dysplasia Bowing of the long bones Hypotelorism Underdeveloped nasal alae Vesicoureteral reflux Polymicrogyria Malabsorption Prominent nasal bridge Craniosynostosis Elbow flexion contracture Hypoplasia of dental enamel Shallow orbits Delayed cranial suture closure Erythroid hypoplasia Everted upper lip vermilion Congenital hypoplastic anemia Parietal foramina Unilateral cleft lip Hypoplastic ilia Vertebral fusion Colon cancer Congenital glaucoma Abnormality of the hand Persistence of hemoglobin F Abnormal dermatoglyphics Hydrops fetalis Webbed neck Nausea Cleft upper lip Nausea and vomiting Narrow chest Pallor Flexion contracture Branchial cyst Elevated red cell adenosine deaminase activity Pachygyria Hyperlordosis Convex nasal ridge Dental malocclusion Triangular face Tapered finger Single transverse palmar crease Thick eyebrow Talipes Synophrys Blepharophimosis Intellectual disability, moderate Bifid thoracic vertebrae Hyperactivity Posteriorly rotated ears Pes cavus Delayed skeletal maturation Clinodactyly Kyphosis Hypoplasia of the corpus callosum Hypoplastic sacral vertebrae Hypoplastic coccygeal vertebrae Transient erythroblastopenia Abnormality of the ureter Coronal craniosynostosis Umbilical hernia Cavum septum pellucidum Abnormality of the shoulder Aplasia/Hypoplasia of the ulna Cervical ribs Generalized tonic-clonic seizures with focal onset Lateral clavicle hook Phocomelia Carpal bone hypoplasia Fibular aplasia Pancreatic cysts Aplasia of the uterus Intermittent thrombocytopenia Fused cervical vertebrae Seborrheic dermatitis Patellar aplasia Allergy Delayed CNS myelination Duodenal atresia Cardiorespiratory arrest Patellar dislocation Nevus flammeus Renal malrotation Edema of the dorsum of hands Focal impaired awareness seizure Fever Hypothyroidism Weight loss Diabetes mellitus Hypogonadism Patent ductus arteriosus Headache Renal insufficiency Respiratory distress Ventriculomegaly Hyperreflexia Aplasia/hypoplasia of the humerus Visual impairment Cow milk allergy Axial malrotation of the kidney Shoulder muscle hypoplasia Tetraphocomelia Lactose intolerance Edema of the dorsum of feet Tibial torsion Amegakaryocytic thrombocytopenia Nevus flammeus of the forehead Megalocornea Intracranial hemorrhage Choanal stenosis Ulnar bowing Limited shoulder movement Perineal fistula Bicoronal synostosis Aplasia of metacarpal bones Flat forehead Urogenital fistula Abnormality of the carpal bones Metopic synostosis Brachyturricephaly Aplasia/Hypoplasia of the patella Carpal bone aplasia Lambdoidal craniosynostosis Limited elbow movement Hand oligodactyly Patellar hypoplasia Anterior plagiocephaly Oxycephaly Sagittal craniosynostosis Bilateral conductive hearing impairment Rib fusion Poikiloderma Persistent cloaca Midface capillary hemangioma Genu varum Decreased antibody level in blood Eosinophilia Adducted thumb Coxa valga Short phalanx of finger Left ventricular hypertrophy Broad thumb Blue sclerae Ventricular hypertrophy Focal-onset seizure Intestinal malrotation Anomalous splenoportal venous system Severe global developmental delay Hepatosplenomegaly Cerebellar hypoplasia Pneumonia Malar flattening Intellectual disability, severe Talipes equinovarus Sensorineural hearing impairment Unilateral radial aplasia Aphalangy of the hands Hypoplastic sacrum



If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like Neuroblastoma and Postaxial hand polydactyly, related diseases and genetic alterations Wide nasal bridge and Primary amenorrhea, related diseases and genetic alterations Visual impairment and Encephalitis, related diseases and genetic alterations Pain and Dental malocclusion, related diseases and genetic alterations

Need help with a diagnosis?

Learn more about how to achieve it with Mendelian


Learn more