Allergic bronchopulmonary aspergillosis
|
(Orphanet:1164)
|
Ataxia-telangiectasia
|
(Orphanet:100)
|
Autosomal dominant hyper-IgE syndrome
|
(Orphanet:2314)
|
BLOOD GROUP, DUFFY SYSTEM
|
(OMIM:110700)
|
CEREBELLAR DEGENERATION-RELATED AUTOANTIGEN 1
|
(OMIM:302650)
|
Chronic mucocutaneous candidiasis
|
(Orphanet:1334)
|
Congenital hypothyroidism due to transplacental passage of maternal TSH-binding inhibitory antibodies
|
(Orphanet:95715)
|
DEFECTIVE INTERFERING PARTICLE INDUCTION, CONTROL OF
|
(OMIM:125260)
|
DEND syndrome
|
(Orphanet:79134)
|
DIABETES MELLITUS, INSULIN-DEPENDENT
|
(OMIM:222100)
|
ECHO VIRUS 11 SENSITIVITY
|
(OMIM:129150)
|
EOSINOPHILOPENIA
|
(OMIM:131430)
|
Epidermodysplasia verruciformis
|
(Orphanet:302)
|
GLOBULIN ANOMALY INVOLVING BETA (2A)-GLOBULIN
|
(OMIM:137900)
|
Hereditary folate malabsorption
|
(Orphanet:90045)
|
IMMUNE SUPPRESSION
|
(OMIM:146850)
|
IMMUNOGLOBULIN D LEVEL IN PLASMA, LOW
|
(OMIM:242890)
|
INOSINE PHOSPHORYLASE DEFICIENCY, IMMUNE DEFECT DUE TO
|
(OMIM:243080)
|
INTRINSIC FACTOR DEFICIENCY
|
(OMIM:261000)
|
Isolated growth hormone deficiency type IA
|
(Orphanet:231662)
|
LYSINE-SPECIFIC DEMETHYLASE 5D
|
(OMIM:426000)
|
Leprosy
|
(Orphanet:548)
|
Lymphoid interstitial pneumonia
|
(Orphanet:79128)
|
METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS
|
(OMIM:250460)
|
MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY
|
(OMIM:608931)
|
Monomelic amyotrophy
|
(Orphanet:65684)
|
Multiple carboxylase deficiency
|
(Orphanet:148)
|
Myeloperoxidase deficiency
|
(Orphanet:2587)
|
Navajo neurohepatopathy
|
(Orphanet:255229)
|
POLIOVIRUS RECEPTOR
|
(OMIM:173850)
|
Permanent neonatal diabetes mellitus
|
(Orphanet:99885)
|
Postsynaptic congenital myasthenic syndromes
|
(Orphanet:98913)
|
Presynaptic congenital myasthenic syndromes
|
(Orphanet:98914)
|
RADIATION SENSITIVITY OF NATURAL KILLER ACTIVITY
|
(OMIM:312210)
|
RAGWEED SENSITIVITY
|
(OMIM:179450)
|
RHEUMATOID ARTHRITIS
|
(OMIM:180300)
|
Reticular dysgenesis
|
(Orphanet:33355)
|
Rheumatic fever
|
(Orphanet:3099)
|
Roussy-Lévy syndrome
|
(Orphanet:3115)
|
SHORT syndrome
|
(Orphanet:3163)
|
SURFACTANT, PULMONARY-ASSOCIATED PROTEIN D
|
(OMIM:178635)
|
SUSCEPTIBILITY TO LYSIS BY ALLOREACTIVE NATURAL KILLER CELLS
|
(OMIM:272370)
|
Schistosomiasis
|
(Orphanet:1247)
|
Synaptic congenital myasthenic syndromes
|
(Orphanet:98915)
|
Syndromic diarrhea
|
(Orphanet:84064)
|
Wolf-Hirschhorn syndrome
|
(Orphanet:280)
|