Disease Browser
Parent Node: Alopecia (D000505) ..Starting node .. Total Hypotrichosis, Mari type (C536973) Child Nodes:
Sister Nodes: ..Alopecia Areata (D000506) 3 ..Alopecia congenita keratosis palmoplantaris (C537050) ..Alopecia contractures dwarfism mental retardation (C537051) ..Alopecia epilepsy oligophrenia syndrome of Moynahan (C537052) ..Alopecia hypogonadism extrapyramidal disorder (C537053) ..Alopecia universalis (C537055) ..Alopecia Universalis Congenita, XY Gonadal Dysgenesis, and Laryngomalacia (C563920) ..Alopecia universalis onychodystrophy vitiligo (C537056) ..Alopecia, Androgenetic, 2 (C567473) ..Alopecia, Androgenetic, 3 (C567317) ..Alopecia, epilepsy, pyorrhea, mental subnormality (C537057) ..Alopecia, Familial Focal (C566301) ..Alopecia, Neurologic Defects, and Endocrinopathy Syndrome (C567425) ..Alopecia-Mental Retardation Syndrome 1 (C565965) ..Alopecia-Mental Retardation Syndrome 2 (C563668) ..ALOPECIA-MENTAL RETARDATION SYNDROME 3 (OMIM:613930) ..Alopecia-Mental Retardation Syndrome with Convulsions and Hypergonadotropic Hypogonadism (C563370) ..Atrichia with Papular Lesions (C565924) ..Bullous Dystrophy, Hereditary Macular Type (C563065) ..Cataract, alopecia, sclerodactyly (C535336) ..Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (C563990) ..Congenital alopecia X-linked (C535981) ..Dermatopathia pigmentosa reticularis (C535374) ..Ectodermal dysplasia alopecia preaxial polydactyly (C538016) ..Ectodermal Dysplasia Syndrome with Distinctive Facial Appearance and Preaxial Polydactyly of Feet (C565067) ..Follicular hamartoma alopecia cystic fibrosis (C537071) ..FRONTONASAL DYSPLASIA 2 (OMIM:613451) ..Garret Tripp syndrome (C535646) ..Glomerulonephritis sparse hair telangiectases (C536825) ..Gomez Lopez Hernandez syndrome (C537285) ..Growth retardation, Alopecia, Pseudoanodontia and Optic atrophy (C535642) ..Hypergonadotropic Hypogonadism And Partial Alopecia (C567109) ..Ichthyosis follicularis atrichia photophobia syndrome (C536085) ..Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis (C564365) ..Jagell Holmgren Hofer syndrome (C537364) ..Johnson neuroectodermal syndrome (C535882) ..Keratosis Follicularis Spinulosa Decalvans, Autosomal Dominant (C567553) ..Kuster Majewski Hammerstein syndrome (C538125) ..Loose Anagen Hair Syndrome (D058247) 2 ..Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis (C567770) ..Microcephaly sparse hair mental retardation seizures (C537545) ..Moloney syndrome (C535810) ..Mucinosis, Follicular (D000507) ..PARC syndrome (C537174) ..Patel Bixler syndrome (C536306) ..Perniola Krajewska Carnevale syndrome (C536660) ..Satoyoshi syndrome (C536616) ..Scholte syndrome (C536638) ..Slti Salem syndrome (C536673) ..T-cell immunodeficiency, congenital alopecia and nail dystrophy (C536781) ..Thumb Deformity And Alopecia (C566054) ..Thumb deformity, alopecia, pigmentation anomaly (C536904) ..Total Hypotrichosis, Mari type (C536973) ..Urban Schosser Spohn syndrome (C536476) ..Woodhouse Sakati syndrome (C536742) ..Woolly hair, hypotrichosis, everted lower lip and outstanding ears (C536746) Human Disease MESH is developed by UMLS . Further data from MedGen , OMIM , CTD
Term ID: 11168
Name: Total Hypotrichosis, Mari type
Definition:
Alternative IDs:
ParentIDs: MESH:D000505
TreeNumbers: C17.800.329.937.122/C536973 |C23.300.035/C536973
Synonyms: Alopecia Universalis Congenita, Mari type |Hypotrichosis, Autosomal Recessive |Hypotrichosis, Localized, Autosomal Recessive, 2 |Hypotrichosis, Total, Mari Type |Mari type Alopecia universalis congenita
Slim Mappings: Pathology (anatomical condition)|Skin disease
Reference:
MedGen: C536973
MeSH: C536973
OMIM: Genes: Phenotypes Disease Causing ClinVar Variants