|
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 inhertitance 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.] |
|
distal myopathy
|
DOID_11720 |
[A muscular dystrophy that is characterized by predominant weakness and atrophy beginning in the feet and/or hands.] |
|
Miyoshi muscular dystrophy 1
|
DOID_0070199 |
[A Miyoshi muscular dystrophy that has_material_basis_in mutation in the DYSF gene on chromosome 2p13.] |
|
infantile-onset distal myopathy
|
DOID_0070196 |
[A distal myopathy that is characterized by autosomal dominant inheritance, infantile onset and progressive disease development.] |
|
distal myopathy 1
|
DOID_0070197 |
[A distal myopathy that is characterized by autosomal dominant inheritance that has_material_basis_in mutation in the MYH7 gene on chromosome 14q11.2.] |
|
autosomal recessive chronic granulomatous disease 3
|
DOID_0070194 |
[A chronic granulomatous disease characterized by that autosomal recessive inheritance has_material_basis_in mutation in the NCF4 gene on chromosome 22q12.] |
|
X-linked chronic granulomatous disease
|
DOID_0070195 |
[A chronic granulomatous disease characterized by X-linked inheritance that has_material_basis_in mutation in the CYBB gene on chromosome Xp21.1-p11.4.] |
|
autosomal recessive chronic granulomatous disease 1
|
DOID_0070192 |
[A chronic granulomatous disease characterized by autosomal recessive inheritance that has_material_basis_in mutation in the NCF1 gene on chromosome 7q11.23.] |
|
autosomal recessive chronic granulomatous disease 4
|
DOID_0070193 |
[A chronic granulomatous disease characterized by autosomal recessive inheritance that has_material_basis_in mutation in the CYBA gene on chromosome 16q24.2.] |
|
Paracoccidioides brasiliensis
|
NCBITaxon_121759 |
|
|
Paracoccidioides
|
NCBITaxon_38946 |
|
|
Lacazia loboi
|
NCBITaxon_121752 |
|
|
spermatogenic failure 18
|
DOID_0070165 |
[A spermatogenic failure that is characterized by sperm flagellar morphological abnormalities that has_material_basis_in homozygous or compound heterozygous mutation in the DNAH1 gene on chromosome 3p21.] |
