All terms in DOID

Label Id Description
Onygenales incertae sedis NCBITaxon_1593277
spermatogenic failure 11 DOID_0070180 [A spermatogenic failure that is characterized by autosomal dominant inheritance of oligozoospermia and in some cases teratozoospermia and/or moderate asthenozoospermia that has_material_basis_in mutation in the KLHL10 gene on chromosome 17q21.]
spermatogenic failure DOID_0111910 [A male infertility characterized by disruption of the process of sperm development from diploid cells into mature haploid spermatozoa.]
Y-linked spermatogenic failure 2 DOID_0070187 [A spermatogenic failure that is characterized by nonobstroctive azoospermia or oligozoospermia that has_material_basis_in interstitial deletions on the Yq11.221 chromosomal region.]
Y-linked monogenic disease DOID_0050738 [A monogenic disease that has_material_basis_in mutations on the Y chromosome.]
spermatogenic failure 1 DOID_0070188 [A spermatogenic failure that is characterized by autosomal recessive inheritance of spermatogenic failure resulting from meiotic defects.]
susceptibility to cutaneous malignant melanoma 1 MIM_155600
X-linked spermatogenic failure 2 DOID_0070185 [A spermatogenic failure that is characterized by meiotic arrest of spermatocytes and mixed testicular atrophy that has_material_basis_in X-linked inheritance of mutation in the TEX11 gene on chromosome Xq13.]
Y-linked spermatogenic failure 1 DOID_0070186 [A Sertoli cell-only syndrome that has_material_basis_in deletions in the Yq11 chromosomal region.]
Sertoli cell-only syndrome DOID_0050457 [A male infertility disease characterized by male sterility, has_material_basis_in azospermia without abnormal sexual development.]
spermatogenic failure 5 DOID_0070183 [A spermatogenic failure that is characterized by autosomal recessive inheritance of large-headed, multiflagellar, polyploid spermatozoa that has_material_basis_in mutation in the AURKC gene on chromosome 19q13.]
susceptibility to cutaneous malignant melanoma 2 MIM_155601
spermatogenic failure 16 DOID_0070184 [A male infertility due to acephalic spermatozoa that is characterized by autosomal recessive inheritance of acephalic spermatozoa that has_material_basis_in mutation in the SUN5 gene on chromosome 20q11.]
male infertility due to acephalic spermatozoa DOID_0112311 [A spermatogenic failure characterized by male infertility caused by a majority of spermatozoa lacking heads.]
spermatogenic failure 23 DOID_0070181 [A spermatogenic failure that is characterized by autosomal recessive inheritance of nonobstructive azoospermia that has_material_basis_in mutation in the TEX14 gene on chromosome 17q23.]
spermatogenic failure 13 DOID_0070182 [A spermatogenic failure that is characterized by autosomal recessive inheritance of azoospermia or oligozoospermia that has_material_basis_in mutation in the TAF4B gene on chromosome 18q11.]
X-linked spermatogenic failure 1 DOID_0070189 [A Sertoli cell-only syndrome characterized by X-linked inheritance.]
obsolete autosomal dominant chronic granulomatous disease DOID_0070190 [A chronic granulomatous disease characterized by autosomal dominant inheritance.]
autosomal recessive chronic granulomatous disease 2 DOID_0070191 [A chronic granulomatous disease characterized by autosomal recessive inheritance that has_material_basis_in mutation in the NCF2 gene on chromosome 1q25.]
Miyoshi muscular dystrophy DOID_0070198 [A distal myopathy that is characterized by autosomal recessive inheritance of distal muscle weakness in the upper and lower limbs that spares the intrinsic muscles of the hands and has onset in young adulthood.]