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| Boli A-Z | | Alopecia
Alopecia, Neurologic Defects, and Endocrinopathy Syndrome
Aniridia 1
Anorexia Nervosa 1
Apert Syndrome
Arthrochalasia Ehlers-Danlos Syndrome
Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus
Baraitser-Winter Syndrome
Baraitser-Winter Syndrome 1
Barber-Say Syndrome
Bifid Nose
Blepharophimosis
Blood Group--Ahonen
Blood Group, I System
Brachydactyly
Cardiofaciocutaneous Syndrome 1
Charcot-Marie-Tooth Disease
Chondroma
Chromosome 16p13.3 Deletion Syndrome, Proximal
Ciliopathy
Cleft Lip
Cornelia De Lange Syndrome
Corpus Callosum, Agenesis of, with Facial Anomalies and Cerebellar Ataxia
Craniosynostosis
Dextrocardia
Diamond-Blackfan Anemia
Ectropion
Encephalocele
Epicanthus
Exotropia
Fanconi Anemia, Complementation Group E
Hepatic Adenomas, Familial
Holoprosencephaly
Hydrocephalus
Hypertelorism, Microtia, Facial Clefting Syndrome
Hypertelorism, Preauricular Sinus, Punctal Pits, and Deafness
Hypertelorism, Teebi Type
Hypertrichosis
Hypospadias
Hypospadias, Hypertelorism, Upper Lid Coloboma, and Mixed-Type Hearing Loss
Hypotonia
Juvenile Myelomonocytic Leukemia
Lentigines
Leopard Syndrome
Macrostomia, Isolated
Mandibulofacial Dysostosis with Macroblepharon and Macrostomia
Mckusick-Kaufman Syndrome
Meningoencephalocele
Microtia
Muenke Syndrome
Myopia
Nasal Encephalocele
Noonan Syndrome 1
Noonan Syndrome with Multiple Lentigines
Opitz-Gbbb Syndrome
Opitz Gbbb Syndrome, Type Ii
Orofacial Cleft
Pilocytic Astrocytoma
Plagiocephaly
Polydactyly
Porencephaly
Preauricular Sinus
Ptosis
Pulmonic Stenosis
Renpenning Syndrome 1
Santos Mateus Leal Syndrome
Say Syndrome
Sclerocornea
Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis
Sotos Syndrome 1
Synostosis
Telecanthus
Tooth Disease
Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 |
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