WormMine

WS297

Intermine data mining platform for C. elegans and related nematodes

Disease Ontology : DOID:0060342 acromelic frontonasal dysostosis Disease Ontology

Namespace  disease_ontology Obsolete  false
Description  A dysostosis characterized by cranium bifidum, severe hypertelorism, median cleft lip and palate, nasal bifurcation, brachycephaly, large fontanelle, tibial hemimelia, preaxial polydactyly of the feet and brain malformations.

1 Ontology

Name
Disease Ontology

12 Parents

Identifier Name Description
DOID:7 disease of anatomical entity A disease that manifests in a defined anatomical structure.
DOID:4 disease A disease is a disposition (i) to undergo pathological processes that (ii) exists in an organism because of one or more disorders in that organism.
DOID:17 musculoskeletal system disease A disease of anatomical entity that occurs in the muscular and/or skeletal system.
DOID:0080001 bone disease A connective tissue disease that affects the structure or development of bone or causes an impairment of normal bone function.
DOID:65 connective tissue disease A musculoskeletal system disease that affects tissues such as skin, tendons, and cartilage.
DOID:0050177 monogenic disease A genetic disease that is the result of one or more abnormal alleles and may be dominant, semi-dominant, or recessive.
DOID:630 genetic disease A disease that has_material_basis_in genetic variations in the human genome.
DOID:0050736 autosomal dominant disease An autosomal genetic disease that is characterized by the presence of one disease-associated mutation of a gene which is sufficient to cause the disease.
DOID:0050739 autosomal genetic disease A monogenic disease that has_material_basis_in a mutation in a single gene on one of the non-sex chromosomes.
DOID:0080006 bone development disease A bone disease that results_in abnormal growth and development located_in bone or located_in cartilage.
DOID:1934 dysostosis A bone development disease that results in defective ossification of bone.
DOID:0060342 acromelic frontonasal dysostosis A dysostosis characterized by cranium bifidum, severe hypertelorism, median cleft lip and palate, nasal bifurcation, brachycephaly, large fontanelle, tibial hemimelia, preaxial polydactyly of the feet and brain malformations.

11 Relations

Relationship
Parent Term . Identifier

Child Term . Identifier
is_a DOID:1934 DOID:0060342
is_a DOID:0050736 DOID:0060342
is_a DOID:17 DOID:0060342
is_a DOID:7 DOID:0060342
is_a DOID:4 DOID:0060342
is_a DOID:0050177 DOID:0060342
is_a DOID:0080006 DOID:0060342
is_a DOID:630 DOID:0060342
is_a DOID:65 DOID:0060342
is_a DOID:0050739 DOID:0060342
is_a DOID:0080001 DOID:0060342

0 Synonyms