All terms in MONDO
| Label |
Id |
Description |
|
glaucoma 1, open angle, J
|
MONDO_0012101 |
|
|
heterotaxy, visceral, 7, autosomal
|
MONDO_0014762 |
|
|
microcephaly 5, primary, autosomal recessive
|
MONDO_0012106 |
|
|
neuropathy, hereditary sensory and autonomic, adult-onset, with anosmia
|
MONDO_0012107 |
|
|
cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2
|
MONDO_0014768 |
|
|
cerebral arteriopathy with subcortical infarcts and leukoencephalopathy
|
MONDO_0007432 |
|
|
Seckel syndrome 9
|
MONDO_0014767 |
|
|
partial lipodystrophy
|
MONDO_0027767 |
|
|
acquired lipodystrophy
|
MONDO_0020089 |
|
|
granulomatosis with polyangiitis
|
MONDO_0012105 |
|
|
Anti-neutrophil cytoplasmic antibody-associated vasculitis
|
MONDO_0015492 |
|
|
leukodystrophy and acquired microcephaly with or without dystonia;
|
MONDO_0014766 |
|
|
reticulate pigment disorder
|
MONDO_0000118 |
|
|
obsolete hereditary pediatric Behçet-like disease
|
MONDO_0014761 |
|
|
TFRC-related combined immunodeficiency
|
MONDO_0014760 |
|
|
obsolete histidinuria-renal tubular defect syndrome
|
MONDO_0026754 |
|
|
adamantinous craniopharyngioma
|
MONDO_0002787 |
|
|
obsolete focal facial dermal dysplasia
|
MONDO_0000124 |
|
|
obsolete factor V and Factor VIII, combined deficiency of
|
MONDO_0000123 |
|
|
papillary craniopharyngioma
|
MONDO_0002788 |
|
