Concept information
Preferred term
Dominant hereditary disorder, NOS
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Narrower concepts
- Aase syndrome
- Achondroplasia
- Acrocephalosyndactyly (Apert)
- Acrodysostosis
- Arteriohepatic dysplasia
- Asymmetric crying face association
- Autosomal dominant deficiency of plasminogen
- Autosomal dominant excess of transthyretin
- Autosomal dominant hypohidrotic ectodermal dysplasia syndrome
- Autosomal dominant hypophosphataemic bone disease
- Autosomal dominant thrombocytopenia with platelet secretion defect
- Autosomal dominant variant form of albumin
- Axenfeld anomaly
- Benign autosomal dominant osteopetrosis
- Bilateral hypoplasia of tibia and postaxial polydactyly syndrome (disorder)
- Brachydactyly and arterial hypertension syndrome (disorder)
- Cardiospondylocarpofacial syndrome (disorder)
- Cataract glaucoma syndrome (disorder)
- Cleft palate, large ears, small head syndrome
- Cleidocranial dysostosis
- Congenital aplasia of lacrimal gland co-occurrent with congenital aplasia of salivary gland (disorder)
- Congenital dyserythropoietic anemia, type III
- Congenital myotonia, autosomal dominant form
- Congenital reticular ichthyosiform erythroderma (disorder)
- Crouzon syndrome
- Deficiency of phosphoserine aminotransferase (disorder)
- Dentatorubropallidoluysian degeneration
- Diaphyseal dysplasia
- Dominant autosomal hereditary disorder, complete penetrance
- Dominant autosomal hereditary disorder, incomplete penetrance
- Dominant hereditary optic atrophy
- Familial amyloid nephropathy with urticaria AND deafness
- Familial amyloid neuropathy, Finnish type
- Familial amyloid polyneuropathy
- Familial benign pemphigus
- Familial hemiplegic migraine
- Familial hypokalemic periodic paralysis
- Familial porphyria cutanea tarda
- Gorlin syndrome
- Granular corneal dystrophy
- Hereditary breast and ovarian cancer syndrome (disorder)
- Hereditary elliptocytosis due to abnormal protein 4.1
- Hereditary elliptocytosis due to alpha spectrin defect
- Hereditary elliptocytosis due to beta spectrin defect in self-association
- Hereditary elliptocytosis due to deficiency of protein 4.1
- Hereditary nephrogenic diabetes insipidus
- Hereditary oculoleptomeningeal amyloid angiopathy
- Hereditary stomatocytosis
- HNSHA due to triosephosphate isomerase deficiency
- Holt-Oram syndrome
- Hyaline dystrophy of Bruch's membrane
- Knuckle pads, deafness AND leukonychia syndrome
- Larsen syndrome
- Marshall-Smith syndrome
- Melnick-Fraser syndrome
- Multiple endocrine neoplasia, type 3
- Mutilating keratoderma
- Nail-patella syndrome
- Neurofibromatosis, type 1
- Neurofibromatosis, type 2
- Noonan syndrome-like disorder with loose anagen hair (disorder)
- Osler hemorrhagic telangiectasia syndrome
- Osteosarcoma, limb anomalies, erythroid macrocytosis syndrome
- Parietal foramina with clavicular hypoplasia
- Peutz-Jeghers syndrome
- Pfeiffer syndrome
- Pseudohypoaldosteronism, type 1, dominant form
- Pseudohypoparathyroidism type I A
- Pseudo von Willebrand disease
- Rieger syndrome
- Scalp, ear, nipple syndrome (disorder)
- Schmitt Gillenwater Kelly syndrome
- Shokeir syndrome
- Splenogonadal fusion, limb defect, micrognathia syndrome (disorder)
- von Willebrand disease type 1
- XTE syndrome
In other languages
-
Persian
URI
http://www.irandoc.acir/onto/irandoc/11164009
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