|
hemorrhage into skin
|
SYMP_0000751 |
|
|
obsolete major affective disorder 1
|
DOID_0080220 |
|
|
laryngeal nerve
|
UBERON_0035642 |
|
|
pineal region germinoma
|
DOID_7428 |
|
|
malignant pineal area germ cell neoplasm
|
DOID_1660 |
|
|
childhood brain germinoma
|
DOID_7429 |
[A brain germinoma that is characterized by tumor of the germ cell in childhood that has_material_basis_in abnormally proliferating cells derives_from germ cells, located_in pineal area and located_in suprasellar area.] |
|
autosomal dominant intellectual developmental disorder 45
|
DOID_0080236 |
[An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in the CIC gene on chromosome 19q13.] |
|
autosomal dominant intellectual developmental disorder 46
|
DOID_0080237 |
[An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in the KCNQ5 gene on chromosome 6q14.] |
|
vascular alteration
|
SYMP_0000769 |
|
|
autosomal dominant intellectual developmental disorder 47
|
DOID_0080238 |
[An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in the STAG1 gene on chromosome 3q22.] |
|
secondary hypertrophic osteoarthropathy
|
DOID_10393 |
|
|
autosomal recessive intellectual developmental disorder 61
|
DOID_0080239 |
[An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the RUN and SH3 domain containing 2 gene (RUSC2) on chromosome 9p13.] |
|
subconjunctival bleeding
|
SYMP_0000767 |
|
|
autosomal dominant intellectual developmental disorder 51
|
DOID_0080232 |
[An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in the KMT5B gene on chromosome 11q13.] |
|
testicular pain
|
SYMP_0000768 |
[A pain that is characterized by a pain in, or about, a testis (testicle) or testes. Testicular pain can be caused by nerve damage, sexually transmitted infections, gangrene, swelling, hernia, kidney stones, inflammation, enlarged veins, fluid in the testicle, or a severe condition known as testicular torsion.] |
|
autosomal dominant intellectual developmental disorder 50
|
DOID_0080233 |
[An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in the NAA15 gene on chromosome 4q31.] |
|
sensory disturbance
|
SYMP_0000765 |
|
|
Clark-Baraitser syndrome
|
DOID_0080234 |
[An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in the TRIP12 gene on chromosome 2q36.] |
|
slow pulse
|
SYMP_0000766 |
|
|
autosomal dominant intellectual developmental disorder 48
|
DOID_0080235 |
[An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in the RAC1 gene on chromosome 7p22.] |
