Human Disease Ontology

Last uploaded: March 2, 2018
Preferred Name

hypotrichosis 1

Synonyms

Hypt1

hereditary generalized hypotrichosis simplex

Hhs

Hts

Definitions

A hypotrichosis that has_material_basis_in a autosomal dominant mutation of APCDD1 on chromosome 18p11.22.

ID

http://purl.obolibrary.org/obo/DOID_0110698

database_cross_reference

OMIM:605389

definition

A hypotrichosis that has_material_basis_in a autosomal dominant mutation of APCDD1 on chromosome 18p11.22.

has_exact_synonym

Hypt1

hereditary generalized hypotrichosis simplex

Hhs

Hts

has_obo_namespace

disease_ontology

id

DOID:0110698

label

hypotrichosis 1

notation

DOID:0110698

prefLabel

hypotrichosis 1

treeView

http://purl.obolibrary.org/obo/DOID_4535

subClassOf

http://purl.obolibrary.org/obo/DOID_4535

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Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/MONDO_0011549 MONDO LOOM
http://purl.obolibrary.org/obo/MONDO_0011549 MONDO LOOM
http://purl.bioontology.org/ontology/OMIM/605389 OMIM LOOM
http://identifiers.org/omim/605389 RETO LOOM
http://identifiers.org/omim/605389 GEXO LOOM
http://identifiers.org/omim/605389 REXO LOOM
http://purl.obolibrary.org/obo/DOID_0110698 MONDO SAME_URI
http://purl.obolibrary.org/obo/DOID_0110698 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_0110698 NIFSTD SAME_URI